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The Biomarker Diseases Diagnosis Blood Tests from Bertis Inc. utilise a proteomic biomarker reagent formulated as a multi-analyte immunological composition. Designed for clinical laboratory and hospital deployment, the kit enables rapid early-stage detection of major diseases through quantitative measurement of disease-specific proteins in blood samples. The technology requires only trace volumes, a few drops of blood, to perform analysis, making it suitable for universal primary screening protocols. The product is available in bulk packaging for B2B distribution and requires cold chain storage throughout the supply chain.
The reagent system employs multi-biomarker immunoassay technology, combining antibodies against multiple protein targets to achieve high sensitivity and specificity in disease detection. Proteomics-based diagnosis identifies proteins specifically expressed in disease states and quantifies their concentrations in patient blood samples. The immunological composition is manufactured to IVD regulatory standards for international export, though buyers should confirm the exact regulatory classification (CE-IVD, FDA 510(k), or KFDA approval) applicable to their destination market. Cold chain integrity, typically maintained at 2-8°C, is critical to preserving reagent stability and assay performance.
Target buyers include clinical diagnostic laboratories, hospital central laboratories, reference laboratories, and IVD distributors serving healthcare systems. The assay format supports high-throughput workflows in early screening programmes for oncology, cardiovascular disease, and metabolic disorders. Buyers should confirm minimum order quantities, shelf life upon delivery, and the supplier's capacity for lot-to-lot consistency documentation. Incoterms, lead times, and freight arrangements for temperature-controlled shipment from Gyeonggi-Do to the buyer's port require direct negotiation with Bertis Inc.
| Reagent Composition | Proteomic Biomarker Reagent (Multi-Analyte Immunological Composition) |
| Sample Volume Required | Trace sample, few drops of blood (standard for proteomics-based diagnostics) |
| Detection Technology | Multi-biomarker immunoassay with quantitative protein measurement |
| Intended Use Environment | Clinical laboratory and hospital diagnostic settings |
| Storage Condition | Cold chain, 2-8°C typical for IVD reagents of this class |
| Regulatory Framework | IVD regulatory standards compliance (buyer to confirm CE-IVD, FDA, or KFDA status) |
| Packaging Format | Bulk packaging for B2B distribution (specific unit configurations to confirm with supplier) |
| Diagnostic Application | Early-stage disease detection via disease-specific protein biomarker quantification |
| Throughput Compatibility | High-throughput laboratory workflow compatible (standard for automated immunoassay platforms) |
| Shelf Life | Typical 12-24 months from manufacture for cold-chain IVD reagents; confirm with Bertis Inc. |
Bertis Inc. is headquartered at 3rd Floor, B Building, 33 Gwacheon-daero 7-gil, Gwacheon-Si, Gyeonggi-Do, 13840, South Korea. The company holds a harbor trust tier on the platform, indicating a verified business registration with foundational credibility signals. The response rate is recorded at 0.00 percent with zero average response hours, which suggests either a new listing or limited historical transaction data through this channel. Buyers should initiate direct contact to assess responsiveness and technical support capabilities.
The supplier's profile focuses exclusively on proteomics-based diagnostic technology, with particular emphasis on multi-biomarker blood tests for early disease detection. No information is provided about manufacturing facility scale, ISO 13485 certification status, headcount, annual revenue, or named client institutions. The company does not state years in operation, previous export markets, or distribution partnerships. Buyers are advised to request documentation of quality management system certification, clinical validation data, and reference installations before committing to supply agreements.
This proteomics-based biomarker diagnostic kit enables rapid early-stage detection of major diseases through advanced blood test analysis. Designed for clinical laboratory and hospital use, the kit employs multi-biomarker immunoassay technology for high sensitivity and specificity. Available in bulk packaging for B2B distribution, the product requires cold chain storage and complies with IVD regulatory standards for international export and import trade.
| Business Type | Supplier |
| Year Established | Recently Joined |
| Employees | Contact Supplier |
| Annual Revenue | Contact Supplier |
| Main Products | View Products Tab |
| Major Markets | Global |
| Response Time | <4h |
| Response Rate | New Supplier |
Before placing an order with Bertis Inc., verify the complete regulatory dossier including current ISO 13485 certification, product-specific CE-IVD or FDA documentation, and any notified body certificates relevant to your market. Request clinical validation data from peer-reviewed studies or investigational use, and confirm that the biomarker panel addresses the disease prevalence in your target population. Ask for reference customers in comparable markets and arrange a video facility tour or third-party audit if the supplier relationship will become strategic. Evaluate the cold chain logistics capability from Gyeonggi-Do to your destination, including the supplier's experience with temperature-controlled international freight.
Lead times, Incoterms, and payment terms must be confirmed directly with Bertis Inc., as no standard terms are published. For diagnostic reagents with cold chain requirements, FCA Incheon or CIP terms are common, though DDP may be preferable for buyers lacking import logistics infrastructure. Payment structures for first orders typically involve advance payment or documentary credit; establish whether open account terms become available after relationship development. Freight forwarders experienced in pharmaceutical and IVD cold chain should be engaged, with contingency planning for customs clearance delays that could compromise temperature-sensitive inventory. Insurance covering product degradation during transit is advisable.
Upon receipt, inspect shipment integrity immediately: verify data logger records for temperature maintenance within 2-8°C, check packaging for damage or thaw indications, and confirm lot numbers match documentation. Perform incoming quality testing including positive and negative controls before patient sample analysis. Retain samples from each lot for potential recall investigation. Documentation should include certificate of analysis, material safety data sheet, instructions for use in your required language, and import customs declarations. Establish a periodic audit schedule with Bertis Inc. to review complaint trends, corrective actions, and any changes to manufacturing process or formulation that could affect assay performance.
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When sourcing Biomarker Diseases Diagnosis Blood Tests for your business, securing the right balance of quality and cost is essential. Bertis Inc., a verified supplier based in South Korea (Republic Of Korea), offers this product with key specifications including In-Vitro Diagnostic (IVD) Biomarker Test Kit, ELISA / Immunochromatography (Lateral Flow), and Whole Blood, Serum, or Plasma. By purchasing directly from the manufacturer or authorized exporter, buyers can negotiate favorable FOB prices starting at $4518025100./Unit and manage bulk orders with a minimum order quantity (MOQ) of 1 Unit. This product is actively traded under HS Code 3822.00, making it a staple in the Diagnostic Kits sector with strong demand from importing countries worldwide.
Importing Biomarker Diseases Diagno requires careful attention to shipping logistics, customs compliance, and secure payment terms. Bertis Inc. offers flexible shipping options such as Full Container Load (FCL) or Less than Container Load (LCL) via sea freight. To ensure a smooth transaction, buyers should verify import duties for HS Code 3822.00 in their destination country. Common payment methods for international B2B transactions include Letter of Credit (L/C), Telegraphic Transfer (T/T), and Documents against Payment (D/P). All transactions and RFQs are facilitated through EximNext, a leading online B2B marketplace designed to make cross-border trade secure and efficient.
Finding trustworthy partners is the foundation of successful importing. The supplier of this Biomarker Diseases Diagno has been verified on our platform. Whether you are a distributor, wholesaler, or procurement manager, you can request a free quotation, ask for product samples, and finalize your bulk purchase with confidence. EximNext hosts thousands of verified manufacturers and exporters across 200+ countries. Explore similar products in the Diagnostic Kits category and connect with top-tier exporters on our comprehensive B2B marketplace. Start your sourcing journey today.
Importing Biomarker Diseases Diagno requires careful attention to shipping logistics, customs compliance, and secure payment terms. Common shipping options include Full Container Load (FCL) or Less than Container Load (LCL) via sea freight. Buyers should verify import duties for HS Code 3822.00 in their destination country. Common payment methods include Letter of Credit (L/C), Telegraphic Transfer (T/T), and Documents against Payment (D/P).
The current listed wholesale price for Biomarker Diseases Diagnosis Blood Tests from Bertis Inc. is $4518025100./Unit on FOB terms from South Korea (Republic Of Korea). Prices may vary depending on order volume, packaging, and destination. For the most accurate bulk quote, send a direct RFQ to Bertis Inc. through EximNext.
The supplier, Bertis Inc., has set a Minimum Order Quantity (MOQ) of 1 Unit for Biomarker Diseases Diagno. For sample requests or smaller trial orders, contact the supplier directly through our platform's inquiry system.
For international shipping and customs clearance, Biomarker Diseases Diagnosis Blood Tests is classified under HS Code 3822.00. Buyers should verify their local customs regulations to determine applicable import duties and taxes for this classification.
To import Biomarker Diseases Diagno from South Korea (Republic Of Korea), negotiate shipping terms (FOB, CIF, or EXW) directly with Bertis Inc.. Ensure you have the necessary import licenses for Diagnostic Kits products in your destination country.
Yes, Bertis Inc. is a verified supplier on EximNext. You can view their complete company profile, business registration details, certifications, and export history before placing a bulk order.
The key specifications for Biomarker Diseases Diagnosis Blood Tests supplied by Bertis Inc. include In-Vitro Diagnostic (IVD) Biomarker Test Kit, ELISA / Immunochromatography (Lateral Flow), and Whole Blood, Serum, or Plasma. For a complete technical data sheet or Certificate of Analysis (COA), send an inquiry directly to the supplier through EximNext.
Bertis Inc. offers Biomarker Diseases Diagno with standard export packaging. Custom packaging, private labeling, and OEM/ODM options may also be available for large wholesale orders.
Biomarker Diseases Diagno is actively imported by buyers worldwide. Request a destination-specific CIF or CFR quote from Bertis Inc. through our platform.
Bertis Inc. maintains international quality certifications. These ensure that the Biomarker Diseases Diagno meets international quality, safety, and regulatory standards required for cross-border trade.
Click "Request Quotation" on this product page, specify your required quantity, preferred shipping terms, and destination country. Bertis Inc. will respond with a detailed wholesale quote including FOB pricing, lead time, and payment options.
Common payment methods include Letter of Credit (L/C), Telegraphic Transfer (T/T), Documents against Payment (D/P), and Escrow services. Confirm accepted terms directly with Bertis Inc..
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