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Infusion intravenous

I have found results from10000+products and3000+suppliers aboutInfusion intravenous

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: Infusion Set
Type: Inorganic Chemicals
Type: Organic Chemicals
Type: Biological Products
Type: Puncture Needle
Material: Plastic
Ethylene Oxide Sterilization
Group: Adult
Without Logo Printing
Application: Internal Medicine
Suitable for: Elderly
State: Liquid
Pharmaceutical Technology: Chemical Synthesis
Quality Guarantee Period: Two Years
Sterilization: Sterilization
Volume: 5ml
Feature: Disposable
Certification: CE
Needle: With Needle
High Precision Experiments
Disinfection: Disinfection
Color: Transparent
With Logo Printing
Application: Surgery
Application: Medical
Suitable for: Adult
Suitable for: Children
Certification: ISO13485
Certification: ISO
Syringe Use: Samples
Syringe Use: Mixing Potions
Syringe Use: Pumping Water
Syringe Use: Intramuscular Injection

Sourcing guidance for Infusion Intravenous

What are the critical technical specifications to consider when sourcing IV infusion sets?

Buyers must prioritize medical-grade materials, specifically DEHP-free or PVC-free tubing to prevent chemical leaching, especially for sensitive patients. Key components include the drip chamber (20 or 60 drops/ml), a high-precision flow regulator, and luer lock connectors to ensure secure, leak-proof attachments. For specialized applications, look for sets with integrated 0.2-micron filters to remove air bubbles and particulates.

Which international compliance standards are mandatory for IV equipment?

As Class II or Class III medical devices, products must adhere to ISO 8536-4 (Infusion equipment for medical use). Suppliers must hold ISO 13485 certification for medical device quality management. For market entry, ensure the products carry CE Marking (MDR 2017/745) for Europe or FDA 510(k) clearance for the United States. All items must be EO (Ethylene Oxide) sterilized with valid sterilization certificates.

How can I verify the quality and safety of the infusion sets before bulk shipment?

Request a Type Test Report from a third-party lab covering tensile strength, leakage tests, and flow rate accuracy. It is essential to verify the shelf life (typically 3-5 years) and ensure the blister packaging maintains its sterile barrier integrity. For large orders, hiring an inspector to perform a bioburden test and a pyrogenicity test is highly recommended to ensure the products are non-toxic.

What are the usage scenarios and functional variations for different IV sets?

Sourcing should be tailored to the clinical need: Gravity Infusion Sets for standard hydration, Burette Sets (Pediatric) for precise volume control in children, and Light-proof (Opaque) Sets for photosensitive medications like vitamins or chemotherapy drugs. Ensure the needle gauge (18G to 27G) matches the intended patient demographic and fluid viscosity.

Cross-Border Procurement Strategy for Medical Consumables

What are the primary risks when importing medical IV sets across borders?

The biggest risk is Customs Seizure due to incomplete medical registration documents. Always ensure the supplier is listed on the White List of the China Chamber of Commerce for Import & Export of Medicines & Health Products (CCCMHPIE). Additionally, sterility compromise during long-transit shipping is a risk; ensure the outer cartons are double-corrugated and moisture-proof.

How should I negotiate with suppliers on Made-in-China.com for long-term medical supply?

Focus on batch consistency rather than just the lowest price. Negotiate for a fixed price contract for 6-12 months to hedge against raw material (plastic resin) fluctuations. Demand a Quality Agreement that specifies the manufacturer cannot change raw material suppliers without prior notification. For high volumes, aim for MOQs that align with full container loads (FCL) to reduce per-unit sterilization and shipping costs.

What transaction security measures should be taken for medical device procurement?

Utilize Secured Trading Services on Made-in-China.com to ensure payment is only released after the Pre-Shipment Inspection (PSI) is passed. Never wire full payments upfront to unverified accounts; use Letter of Credit (L/C) for large-scale medical tenders to mitigate financial risk.

What are the logistics requirements for shipping sterile medical supplies to international markets?

Products must be shipped in temperature-controlled environments if possible, avoiding extreme heat which can degrade plastic components. Ensure the Shipping Mark includes the 'Sterile' symbol and 'Keep Dry' icons according to ISO 780. For sea freight, use pallets with plastic wrap to prevent floor moisture from affecting the sterile paper-plastic pouches.

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