Hebei Highrang Biotechnology Co,. Ltd — Verified Supplier

About Hebei Highrang Biotechnology Co,. Ltd - Rapid Test Kits Supplier in China

Hebei Highrang Biotechnology Co,. Ltd is based in China and currently lists six active products across medical and diagnostic categories. The catalogue includes a 3‑layer disposable surgical face mask classified under HS code 6307.90 and made from polypropylene non‑woven fabric. A neutralizing antibody test kit is listed under HS code 3822.00 and uses immunochromatographic reagents on a nitrocellulose membrane with fluorescent conjugates. The company also offers a diesel vehicle urea solution in 10 L containers, though no HS code is provided in the catalogue. A blood pressure meter (HS 9018.90) with an ABS plastic housing and electronic components is part of the range, as is a medical‑grade digital thermometer (HS 9025.19) built from ABS plastic and electronics. Finally, a COVID‑19 antigen rapid test saliva pen is listed under HS code 3822.00, featuring a lateral‑flow nitrocellulose membrane, monoclonal antibody conjugates, and a foam‑tip saliva swab.

Product Range and Specialties of Hebei Highrang Biotechnology Co,. Ltd

The product portfolio covers three main segments: personal protective equipment, point‑of‑care diagnostic kits, and electronic medical devices. The disposable surgical mask follows the typical three‑layer structure (outer spunbond PP, middle melt‑blown filter, inner soft PP) that meets standards such as ASTM F2100 and EN 14683, with bacterial filtration efficiency (BFE) commonly rated at 95 % or higher. Rapid test kits, both the neutralizing antibody and COVID‑19 antigen formats, employ lateral‑flow technology; standard performance metrics include sensitivity above 90 % and specificity above 95 % when validated against reference methods. The diesel‑vehicle urea solution is a 32.5 % aqueous urea (AdBlue) solution, the standard concentration required for selective catalytic reduction systems. Blood pressure meters and digital thermometers are classified as medical devices under IEC 60601‑1, typically offering measurement accuracies of ±3 mm Hg for pressure and ±0.1 °C for temperature respectively. Each device is housed in ABS plastic, a material chosen for its impact resistance and compliance with medical‑device safety regulations.

Trade and Export Information - Hebei Highrang Biotechnology Co,. Ltd

China is a leading exporter of medical consumables and point‑of‑care diagnostics, supplying North America, the European Union, and Southeast Asian markets. HS chapter 63 (e.g., 6307.90) covers protective clothing and masks, which are subject to customs inspection for compliance with safety standards and may require CE marking for EU entry. HS chapter 38 (3822.00) encompasses diagnostic or laboratory reagents, where importers often demand certificates of analysis, CE conformity, and, for the United States, FDA Emergency Use Authorization documentation. Electronic medical devices listed under HS 9018.90 and 9025.19 are typically shipped in 20‑ft or 40‑ft containers with protective packaging to prevent static discharge; they frequently need a Declaration of Conformity and an ISO 13485 quality‑management certificate from the exporter. The urea solution, while not assigned an HS code in the catalogue, usually falls under HS 2836.20 and is regulated under the Rotterdam Convention for hazardous chemicals, requiring material safety data sheets (MSDS) and proper labeling for bulk shipment.

Sourcing from Hebei Highrang Biotechnology Co,. Ltd - Buyer Guidance

Buyers should request a full set of compliance documents before placing orders: CE Declaration of Conformity for masks and diagnostic kits, ISO 13485 or ISO 9001 certificates for electronic devices, and a Material Safety Data Sheet for the urea solution. For the rapid test kits, a performance validation report showing sensitivity, specificity, limit of detection, and stability data is standard practice. Sample units of the surgical mask and the antigen rapid test are typically offered in quantities of 100 - 500 pieces to verify filtration efficiency and visual result clarity before bulk purchase. Verify that the packaging complies with ISO 11607 for sterile barrier systems when applicable, and confirm that the product is shipped in moisture‑controlled containers to preserve performance of electronic devices and reagents. Lead times for the listed items range from 15 days for the masks to 30 - 45 days for the diagnostic kits, depending on production scheduling and required regulatory approvals.

Frequently Asked Questions About Hebei Highrang Biotechnology Co,. Ltd

What material is used for the 3‑layer disposable surgical face mask and what HS code applies?

The mask is made from polypropylene (PP) non‑woven fabric and is classified under HS code 6307.90, which covers other made‑up textile articles, including protective masks.

Which standards are typically required for the COVID‑19 antigen rapid test saliva pen?

Importers usually require CE marking, a Declaration of Conformity, and a performance validation report that includes sensitivity, specificity, and limit of detection data.

What is the typical concentration and regulatory classification of the diesel vehicle urea solution?

The solution is a 32.5 % aqueous urea (AdBlue) formulation, generally classified under HS code 2836.20 and subject to hazardous‑chemical regulations, requiring an MSDS and proper labeling.

What accuracy specifications are common for the blood pressure meter listed under HS 9018.90?

Blood pressure meters for medical use commonly meet IEC 60601‑1 standards and provide measurement accuracy of ±3 mm Hg across the typical range of 0 - 300 mm Hg.

How should the medical‑grade digital thermometer be packaged for export?

Thermometers are usually packed in anti‑static, moisture‑resistant blister packs or sealed cartons complying with ISO 11607 to protect electronic components during transit.

What documentation should a buyer request for the neutralizing antibody test kit?

Buyers should ask for a CE Declaration of Conformity, ISO 13485 certification, a full analytical report showing reagent stability, and a clinical validation study confirming neutralizing antibody detection performance.

What are typical minimum order quantities (MOQs) for the disposable surgical masks?

Suppliers often set MOQs between 10 000 and 50 000 pieces per order, depending on packaging format and required certification testing.

Which Incoterms are most commonly used for shipping these medical products from China?

CIF (Cost, Insurance, Freight) to major ports and DDP (Delivered Duty Paid) to the buyer’s warehouse are the most frequently applied Incoterms for medical consumables and devices exported from China.

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Hebei Highrang Biotechnology Co,. Ltd

Harbor
Country flag , China
🛡️
55/100
Trust Score

Hebei Highrang Biotechnology Co,. Ltd Product Catalog

Showing 12 of 22 products
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Neutralizing Antibody Test Kit
Harbor
Neutralizing Antibody Test Kit
Contact
MOQ: 1 Unit
COVID-19 Antigen Rapid Test Saliva Pen
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COVID-19 Antigen Rapid Test Saliva Pen
Contact
MOQ: 1 Unit
Novel SARS-CoV-2 Antigen Rapid Test Kit
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Novel SARS-CoV-2 Antigen Rapid Test Kit
Contact
MOQ: 1 Unit
Omicron COVID Test Kit
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Omicron COVID Test Kit
Contact
MOQ: 1 Unit
Rapid SARS-Cov-2 Antigen Test Card
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Rapid SARS-Cov-2 Antigen Test Card
Contact
MOQ: 1 Unit
Non Contact Forehead Thermometer
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Non Contact Forehead Thermometer
Contact
MOQ: 1 Unit
Portable Mesh Nebuliser
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Portable Mesh Nebuliser
Contact
MOQ: 1 Unit
Medical Grade Digital Thermometer
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Medical Grade Digital Thermometer
Contact
MOQ: 1 Unit
Blood Pressure Meter
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Blood Pressure Meter
Contact
MOQ: 1 Unit
Diesel Vehicle Urea Solution 10L
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Diesel Vehicle Urea Solution 10L
Contact
MOQ: 1 Unit
Safety Insulin Syringe With Retractable Needle
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Safety Insulin Syringe With Retractable Needle
Contact
MOQ: 1 Unit
Nasopharyngeal Saliva Antigen Rapid Test Kit
Harbor
Nasopharyngeal Saliva Antigen Rapid Test Kit
Contact
MOQ: 1 Unit

About Hebei Highrang Biotechnology Co,. Ltd - Rapid Test Kits Supplier in China

Hebei Highrang Biotechnology Co,. Ltd is based in China and currently lists six active products across medical and diagnostic categories. The catalogue includes a 3‑layer disposable surgical face mask classified under HS code 6307.90 and made from polypropylene non‑woven fabric. A neutralizing antibody test kit is listed under HS code 3822.00 and uses immunochromatographic reagents on a nitrocellulose membrane with fluorescent conjugates. The company also offers a diesel vehicle urea solution in 10 L containers, though no HS code is provided in the catalogue. A blood pressure meter (HS 9018.90) with an ABS plastic housing and electronic components is part of the range, as is a medical‑grade digital thermometer (HS 9025.19) built from ABS plastic and electronics. Finally, a COVID‑19 antigen rapid test saliva pen is listed under HS code 3822.00, featuring a lateral‑flow nitrocellulose membrane, monoclonal antibody conjugates, and a foam‑tip saliva swab.

Product Range and Specialties of Hebei Highrang Biotechnology Co,. Ltd

The product portfolio covers three main segments: personal protective equipment, point‑of‑care diagnostic kits, and electronic medical devices. The disposable surgical mask follows the typical three‑layer structure (outer spunbond PP, middle melt‑blown filter, inner soft PP) that meets standards such as ASTM F2100 and EN 14683, with bacterial filtration efficiency (BFE) commonly rated at 95 % or higher. Rapid test kits, both the neutralizing antibody and COVID‑19 antigen formats, employ lateral‑flow technology; standard performance metrics include sensitivity above 90 % and specificity above 95 % when validated against reference methods. The diesel‑vehicle urea solution is a 32.5 % aqueous urea (AdBlue) solution, the standard concentration required for selective catalytic reduction systems. Blood pressure meters and digital thermometers are classified as medical devices under IEC 60601‑1, typically offering measurement accuracies of ±3 mm Hg for pressure and ±0.1 °C for temperature respectively. Each device is housed in ABS plastic, a material chosen for its impact resistance and compliance with medical‑device safety regulations.

Trade and Export Information - Hebei Highrang Biotechnology Co,. Ltd

China is a leading exporter of medical consumables and point‑of‑care diagnostics, supplying North America, the European Union, and Southeast Asian markets. HS chapter 63 (e.g., 6307.90) covers protective clothing and masks, which are subject to customs inspection for compliance with safety standards and may require CE marking for EU entry. HS chapter 38 (3822.00) encompasses diagnostic or laboratory reagents, where importers often demand certificates of analysis, CE conformity, and, for the United States, FDA Emergency Use Authorization documentation. Electronic medical devices listed under HS 9018.90 and 9025.19 are typically shipped in 20‑ft or 40‑ft containers with protective packaging to prevent static discharge; they frequently need a Declaration of Conformity and an ISO 13485 quality‑management certificate from the exporter. The urea solution, while not assigned an HS code in the catalogue, usually falls under HS 2836.20 and is regulated under the Rotterdam Convention for hazardous chemicals, requiring material safety data sheets (MSDS) and proper labeling for bulk shipment.

Sourcing from Hebei Highrang Biotechnology Co,. Ltd - Buyer Guidance

Buyers should request a full set of compliance documents before placing orders: CE Declaration of Conformity for masks and diagnostic kits, ISO 13485 or ISO 9001 certificates for electronic devices, and a Material Safety Data Sheet for the urea solution. For the rapid test kits, a performance validation report showing sensitivity, specificity, limit of detection, and stability data is standard practice. Sample units of the surgical mask and the antigen rapid test are typically offered in quantities of 100 - 500 pieces to verify filtration efficiency and visual result clarity before bulk purchase. Verify that the packaging complies with ISO 11607 for sterile barrier systems when applicable, and confirm that the product is shipped in moisture‑controlled containers to preserve performance of electronic devices and reagents. Lead times for the listed items range from 15 days for the masks to 30 - 45 days for the diagnostic kits, depending on production scheduling and required regulatory approvals.

Frequently Asked Questions About Hebei Highrang Biotechnology Co,. Ltd

What material is used for the 3‑layer disposable surgical face mask and what HS code applies?

The mask is made from polypropylene (PP) non‑woven fabric and is classified under HS code 6307.90, which covers other made‑up textile articles, including protective masks.

Which standards are typically required for the COVID‑19 antigen rapid test saliva pen?

Importers usually require CE marking, a Declaration of Conformity, and a performance validation report that includes sensitivity, specificity, and limit of detection data.

What is the typical concentration and regulatory classification of the diesel vehicle urea solution?

The solution is a 32.5 % aqueous urea (AdBlue) formulation, generally classified under HS code 2836.20 and subject to hazardous‑chemical regulations, requiring an MSDS and proper labeling.

What accuracy specifications are common for the blood pressure meter listed under HS 9018.90?

Blood pressure meters for medical use commonly meet IEC 60601‑1 standards and provide measurement accuracy of ±3 mm Hg across the typical range of 0 - 300 mm Hg.

How should the medical‑grade digital thermometer be packaged for export?

Thermometers are usually packed in anti‑static, moisture‑resistant blister packs or sealed cartons complying with ISO 11607 to protect electronic components during transit.

What documentation should a buyer request for the neutralizing antibody test kit?

Buyers should ask for a CE Declaration of Conformity, ISO 13485 certification, a full analytical report showing reagent stability, and a clinical validation study confirming neutralizing antibody detection performance.

What are typical minimum order quantities (MOQs) for the disposable surgical masks?

Suppliers often set MOQs between 10 000 and 50 000 pieces per order, depending on packaging format and required certification testing.

Which Incoterms are most commonly used for shipping these medical products from China?

CIF (Cost, Insurance, Freight) to major ports and DDP (Delivered Duty Paid) to the buyer’s warehouse are the most frequently applied Incoterms for medical consumables and devices exported from China.

About Hebei Highrang Biotechnology Co,. Ltd - Rapid Test Kits Supplier in China

Hebei Highrang Biotechnology Co,. Ltd is based in China and currently lists six active products across medical and diagnostic categories. The catalogue includes a 3‑layer disposable surgical face mask classified under HS code 6307.90 and made from polypropylene non‑woven fabric. A neutralizing antibody test kit is listed under HS code 3822.00 and uses immunochromatographic reagents on a nitrocellulose membrane with fluorescent conjugates. The company also offers a diesel vehicle urea solution in 10 L containers, though no HS code is provided in the catalogue. A blood pressure meter (HS 9018.90) with an ABS plastic housing and electronic components is part of the range, as is a medical‑grade digital thermometer (HS 9025.19) built from ABS plastic and electronics. Finally, a COVID‑19 antigen rapid test saliva pen is listed under HS code 3822.00, featuring a lateral‑flow nitrocellulose membrane, monoclonal antibody conjugates, and a foam‑tip saliva swab.

Product Range and Specialties of Hebei Highrang Biotechnology Co,. Ltd

The product portfolio covers three main segments: personal protective equipment, point‑of‑care diagnostic kits, and electronic medical devices. The disposable surgical mask follows the typical three‑layer structure (outer spunbond PP, middle melt‑blown filter, inner soft PP) that meets standards such as ASTM F2100 and EN 14683, with bacterial filtration efficiency (BFE) commonly rated at 95 % or higher. Rapid test kits, both the neutralizing antibody and COVID‑19 antigen formats, employ lateral‑flow technology; standard performance metrics include sensitivity above 90 % and specificity above 95 % when validated against reference methods. The diesel‑vehicle urea solution is a 32.5 % aqueous urea (AdBlue) solution, the standard concentration required for selective catalytic reduction systems. Blood pressure meters and digital thermometers are classified as medical devices under IEC 60601‑1, typically offering measurement accuracies of ±3 mm Hg for pressure and ±0.1 °C for temperature respectively. Each device is housed in ABS plastic, a material chosen for its impact resistance and compliance with medical‑device safety regulations.

Trade and Export Information - Hebei Highrang Biotechnology Co,. Ltd

China is a leading exporter of medical consumables and point‑of‑care diagnostics, supplying North America, the European Union, and Southeast Asian markets. HS chapter 63 (e.g., 6307.90) covers protective clothing and masks, which are subject to customs inspection for compliance with safety standards and may require CE marking for EU entry. HS chapter 38 (3822.00) encompasses diagnostic or laboratory reagents, where importers often demand certificates of analysis, CE conformity, and, for the United States, FDA Emergency Use Authorization documentation. Electronic medical devices listed under HS 9018.90 and 9025.19 are typically shipped in 20‑ft or 40‑ft containers with protective packaging to prevent static discharge; they frequently need a Declaration of Conformity and an ISO 13485 quality‑management certificate from the exporter. The urea solution, while not assigned an HS code in the catalogue, usually falls under HS 2836.20 and is regulated under the Rotterdam Convention for hazardous chemicals, requiring material safety data sheets (MSDS) and proper labeling for bulk shipment.

Sourcing from Hebei Highrang Biotechnology Co,. Ltd - Buyer Guidance

Buyers should request a full set of compliance documents before placing orders: CE Declaration of Conformity for masks and diagnostic kits, ISO 13485 or ISO 9001 certificates for electronic devices, and a Material Safety Data Sheet for the urea solution. For the rapid test kits, a performance validation report showing sensitivity, specificity, limit of detection, and stability data is standard practice. Sample units of the surgical mask and the antigen rapid test are typically offered in quantities of 100 - 500 pieces to verify filtration efficiency and visual result clarity before bulk purchase. Verify that the packaging complies with ISO 11607 for sterile barrier systems when applicable, and confirm that the product is shipped in moisture‑controlled containers to preserve performance of electronic devices and reagents. Lead times for the listed items range from 15 days for the masks to 30 - 45 days for the diagnostic kits, depending on production scheduling and required regulatory approvals.

Frequently Asked Questions About Hebei Highrang Biotechnology Co,. Ltd
What material is used for the 3‑layer disposable surgical face mask and what HS code applies?
The mask is made from polypropylene (PP) non‑woven fabric and is classified under HS code 6307.90, which covers other made‑up textile articles, including protective masks.
Which standards are typically required for the COVID‑19 antigen rapid test saliva pen?
Importers usually require CE marking, a Declaration of Conformity, and a performance validation report that includes sensitivity, specificity, and limit of detection data.
What is the typical concentration and regulatory classification of the diesel vehicle urea solution?
The solution is a 32.5 % aqueous urea (AdBlue) formulation, generally classified under HS code 2836.20 and subject to hazardous‑chemical regulations, requiring an MSDS and proper labeling.
What accuracy specifications are common for the blood pressure meter listed under HS 9018.90?
Blood pressure meters for medical use commonly meet IEC 60601‑1 standards and provide measurement accuracy of ±3 mm Hg across the typical range of 0 - 300 mm Hg.
How should the medical‑grade digital thermometer be packaged for export?
Thermometers are usually packed in anti‑static, moisture‑resistant blister packs or sealed cartons complying with ISO 11607 to protect electronic components during transit.
What documentation should a buyer request for the neutralizing antibody test kit?
Buyers should ask for a CE Declaration of Conformity, ISO 13485 certification, a full analytical report showing reagent stability, and a clinical validation study confirming neutralizing antibody detection performance.
What are typical minimum order quantities (MOQs) for the disposable surgical masks?
Suppliers often set MOQs between 10 000 and 50 000 pieces per order, depending on packaging format and required certification testing.
Which Incoterms are most commonly used for shipping these medical products from China?
CIF (Cost, Insurance, Freight) to major ports and DDP (Delivered Duty Paid) to the buyer’s warehouse are the most frequently applied Incoterms for medical consumables and devices exported from China.
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Hebei Highrang Biotechnology Co,. Ltd
Country flag , China
Harbor
55/100
Trust Score
📦
22
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