Evolution Med — Supplier
About Evolution Med - Medical & HealthCare Supplier in India
Evolution Med, located in India, offers 5 active products in the medical and healthcare industry. Their product range includes Patient Monitors, Medical & HealthCare, Dental Equipments & Materials, Diagnostic Kits, and CT Scanners. Specifically, their catalogue features a Bis anaesthesia monitor, Fetal Doppler, Dental diode laser, Finger Oximeter, and a GE Hispeed Dxi - Refurbished. The Finger Oximeter, for instance, is classified under the HS code 9018.90 and is made of Medical-Grade ABS Plastic with OLED Display.
Buyers of medical equipment from India, such as Evolution Med, typically source products that meet international standards for quality and safety. The Indian medical devices market is known for its stringent regulatory requirements, with many exporters adhering to standards set by the Central Drugs Standard Control Organisation. The country's export landscape for medical devices is characterized by a strong focus on quality control and assurance.
Product Range and Specialties of Evolution Med
Evolution Med's product range encompasses various medical specialties, including patient monitoring and diagnostic equipment. The Finger Oximeter, with its HS code 9018.90, is a notable example, utilizing Medical-Grade ABS Plastic with OLED Display. In the medical devices industry, exporters of patient monitoring equipment typically adhere to standards such as those set by the International Electrotechnical Commission (IEC) and the International Organization for Standardization (ISO). For instance, the IEC 60601-1 standard for medical electrical equipment is commonly applied. Buyers of these products usually require specifications that meet these standards, ensuring the safety and efficacy of the devices.
Trade and Export Information - Evolution Med
Exporters of medical devices from India, such as Evolution Med, often cater to international markets where these products are in high demand. The HS code 9018.90 for the Finger Oximeter and 9022.12 for the GE Hispeed Dxi - Refurbished indicate the specific product categories that are subject to regulatory oversight. Buyers of medical equipment usually require compliance with standards such as CE marking for the European market or FDA clearance for the US market. The logistics of exporting these goods involve adherence to Incoterms, such as CIF or FOB, and careful packaging to ensure the integrity of the products during transit. Typically, medical devices are shipped in secure, tamper-evident packaging to prevent damage or contamination.
Sourcing from Evolution Med - Buyer Guidance
When sourcing from Evolution Med, buyers should request detailed product specifications, including materials used and compliance with relevant standards such as IEC 60601-1 or ISO 13485. It is also advisable to ask for test reports, certification documents such as CE or FDA certificates, and any relevant clinical data. Verification of the supplier's quality control processes and inspection of the products before shipment can help ensure that the goods meet the required standards. Buyers should also confirm the MOQ and lead time to ensure timely delivery of their orders. Requesting samples can provide an opportunity to assess the product quality firsthand.
Frequently Asked Questions About Evolution Med
What product categories does Evolution Med specialize in?
Evolution Med specializes in Patient Monitors, Medical & HealthCare, Dental Equipments & Materials, Diagnostic Kits, and CT Scanners. Their product range includes a variety of medical devices such as the Bis anaesthesia monitor and the Finger Oximeter.
What is the HS code for the Finger Oximeter?
The HS code for the Finger Oximeter is 9018.90, indicating its classification as a medical device.
What materials are used in the Finger Oximeter?
The Finger Oximeter is made of Medical-Grade ABS Plastic with OLED Display, ensuring durability and safety for medical use.
What are the common certifications required for medical devices like those offered by Evolution Med?
Common certifications required for medical devices include CE marking for the European market, FDA clearance for the US market, and compliance with standards such as IEC 60601-1 or ISO 13485. Buyers should verify which certifications are applicable to the specific products they are sourcing.
How are medical devices typically packaged for export?
Medical devices are typically packaged in secure, tamper-evident packaging to prevent damage or contamination during transit. The packaging should also comply with relevant regulatory requirements, such as those related to the transportation of medical devices.
What Incoterms are commonly used for the export of medical devices?
Incoterms such as CIF (Cost, Insurance, and Freight) or FOB (Free on Board) are commonly used for the export of medical devices, depending on the agreement between the buyer and the seller. Buyers should clarify the Incoterms with the supplier to understand their responsibilities and costs.
Can I request a refund or replacement if the products do not meet specifications?
Buyers should discuss refund or replacement policies with Evolution Med before placing an order. Typically, suppliers have specific procedures for handling defective products or those that do not meet specifications, which may involve repair, replacement, or refund, subject to the terms of the sales contract.





































