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Infusion

I have found results from100000+products and50000+suppliers aboutInfusion

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: Infusion Set
Type: Biological Products
Type: X-Ray Film
Surgical Supplies Materials
Type: Organic Chemicals
Material: Plastic
Without Ethylene Oxide Sterilization
Quality Guarantee Period: One Year
Group: Adult
With Logo Printing
Application: Internal Medicine
For external use
Suitable for: Adult
State: Liquid
Pharmaceutical Technology: Chemical Synthesis
Certification: CE
Medical Device Regulatory Type: Type 3
Shape: Oral Liquid
Ethylene Oxide Sterilization
Quality Guarantee Period: Two Years
Without Logo Printing
For oral administration
Suitable for: Elderly
Suitable for: Children
Certification: SGS
Certification: ISO13485

Sourcing guidance for Infusion

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

Buyers must prioritize medical-grade PVC or DEHP-free materials to ensure patient safety and prevent chemical leaching. Key components include a sharp spike for easy insertion, a transparent drip chamber for flow monitoring, and a high-precision roller clamp for flow rate adjustment. For specialized needs, ensure the presence of a 0.22 or 1.2-micron fluid filter to remove particulates and bacteria.

Which international compliance standards are mandatory for infusion products?

As Class II or Class III medical devices, infusion products must adhere to ISO 13485 (Quality Management Systems for Medical Devices). For global market access, verify CE Marking (MDR 2017/745) for Europe and FDA 510(k) clearance for the United States. Additionally, products must meet ISO 8536-4 standards specifically for infusion equipment for single use.

How can I evaluate the performance and safety of infusion pumps?

Focus on flow rate accuracy (typically within ±5%) and the sensitivity of the occlusion alarm system. The pump should feature air-in-line detection and an anti-free-flow function to prevent accidental bolus. Ensure the battery life supports at least 4-8 hours of continuous operation for mobile patient use.

What are the sterilization requirements for disposable infusion sets?

All disposable infusion sets must be sterilized using Ethylene Oxide (EO) gas or Gamma Radiation. The packaging must be a medical-grade blister pack or PE bag that maintains a sterile barrier for at least 3 to 5 years. Always check the sterilization indicator and expiration date on the batch samples.

Cross-Border Procurement Strategy for Medical Infusion Products

What are the primary risks when importing medical infusion devices?

The biggest risk is customs seizure due to improper documentation or lack of medical device registration in the destination country. Ensure the supplier provides a Certificate of Free Sale (CFS) and a Declaration of Conformity. Another risk is quality degradation during transit; ensure products are shipped in temperature-controlled environments if specific components are heat-sensitive.

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

Start by requesting a factory audit report or a video inspection to verify their Cleanroom (Class 100,000) production environment. Negotiate based on tiered pricing; for medical consumables, a volume increase from 10,000 to 100,000 units can often yield a 15-25% cost reduction. Always insist on a pre-shipment inspection (PSI) by a third party like SGS or Intertek.

What are the recommended shipping and payment security measures?

Use Secured Trading Services on Made-in-China.com to protect your payment until the goods pass quality inspection. For shipping, Sea Freight is most economical for high-volume disposables, but ensure the use of palletized packaging to prevent crushing. For electronic infusion pumps, use Air Freight with shock-absorbent packaging to protect sensitive internal sensors.

How do I ensure alignment with international trade policies for medical goods?

Stay updated on HS Code classification (typically 9018.39 for infusion sets) to determine applicable tariffs. Be aware of Anti-Dumping Duties that some regions may apply to medical plastics. Ensure all labeling, including UDI (Unique Device Identification), complies with the destination country's language and regulatory requirements.

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