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Iv set

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Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Surgical Supplies Materials
Type: Infusion Set
Material: Plastic
Ethylene Oxide Sterilization
Quality Guarantee Period: Two Years
Group: Adult
Without Logo Printing
Sterilization: Sterilization
Application: Medical
Feature: Disposable
Certification: CE
Syringe Use: Intramuscular Injection
Needle: With Needle
Volume: 10ml
Disinfection: Disinfection
Medical Device Regulatory Type: Type 3
Without Ethylene Oxide Sterilization
Group: Children
With Logo Printing
Application: Veterinary
Certification: ISO13485
Certification: FDA
High Precision Experiments

Sourcing guidance for Iv Set

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

Buyers must prioritize medical-grade materials, specifically DEHP-free or PVC-free tubing to prevent chemical leaching. Key components should include a sharp, easy-to-puncture spike, a transparent drip chamber (typically 20 drops/ml or 60 drops/ml for pediatric use), and a high-precision roller clamp for flow rate control. Ensure the needle or luer lock connector meets ISO 80369-7 standards to prevent misconnections.

Which international compliance standards are mandatory for IV sets?

As a Class II medical device, IV sets must adhere to strict regulatory frameworks. Ensure the supplier holds ISO 13485 certification for medical device quality management. Products must be CE Marked (MDR 2017/745) for the European market or have FDA 510(k) clearance for the U.S. Additionally, verify that the sterilization process follows ISO 11135 (Ethylene Oxide sterilization) and that the packaging maintains sterile barrier integrity.

How can I evaluate the functional safety and performance of an IV set?

Request test reports for tensile strength to ensure joints do not leak under pressure, and flow rate consistency tests. The filter membrane (usually 15-micron) must be checked for its ability to prevent particulate matter from entering the bloodstream. For high-end applications, look for needle-free injection sites to reduce the risk of needle-stick injuries for healthcare workers.

What are the usage scenarios and variations I should be aware of?

Sourcing depends on the clinical application: Gravity IV sets are standard for basic fluid delivery, while Burette sets are required for precise pediatric dosing. If the medication is light-sensitive, you must source light-proof (amber-colored) IV sets. For use with infusion pumps, ensure the tubing is compatible with specific pump brands to avoid occlusion alarms or inaccurate dosing.

Cross-Border Procurement & Risk Management for Medical Consumables

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

The greatest risk is Customs Seizure due to inadequate medical registration documents. Always verify that the supplier is registered on the White List of the exporting country's Chamber of Commerce. Another risk is sterility compromise during long-transit shipping; ensure the outer cartons are double-corrugated and moisture-resistant.

How should I negotiate with suppliers on Made-in-China.com?

Focus on Quality Consistency rather than just the lowest price. Request a Pre-Shipment Inspection (PSI) by a third party like SGS or Intertek. Negotiate a staggered payment term (e.g., 30% deposit, 70% after passing lab tests) and ask for OEM/Private Labeling options, as medical branding is crucial for market trust.

What are the logistics and shipping precautions for sterile medical goods?

IV sets are bulky but light, so volumetric weight will impact shipping costs. Use FOB (Free On Board) terms to maintain control over the freight forwarder. Ensure the shipping container is clean and free of odors, as medical plastics can absorb chemical scents. Avoid transshipment in ports with extreme humidity to prevent mold on the paper-plastic sterile pouches.

How can I ensure transaction security for large-scale medical orders?

Utilize Secured Trading Services provided by Made-in-China.com to protect your funds until the goods are verified. Always cross-reference the supplier's business license with their medical device production permit to ensure they are a legitimate manufacturer and not an unlicensed middleman.

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