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0.9% sodium chloride injection

I have found results from700+products and200+suppliers about0.9% sodium chloride injection

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: Organic Chemicals
Type: Inorganic Chemicals
Type: Biological Products
Application: Internal Medicine
Suitable for: Adult
State: Liquid
Pharmaceutical Technology: Chemical Synthesis
For external use
Shape: Oral Liquid
Application: Surgery
Suitable for: Elderly
Suitable for: Children
State: Solid
Shape: Powder

Sourcing guidance for 0.9% Sodium Chloride Injection

What are the essential pharmaceutical standards and certifications required for 0.9% Sodium Chloride Injection?

As a sterile medical product, it must strictly adhere to international pharmacopoeia standards such as USP (United States Pharmacopeia), BP (British Pharmacopeia), or EP (European Pharmacopeia). Suppliers must possess a valid GMP (Good Manufacturing Practice) certificate to ensure the production environment meets sterile requirements. For international trade, look for CE marking (for the EU) or FDA 510(k) clearance (for the US) to ensure legal market entry.

What technical specifications should be prioritized regarding packaging and container integrity?

Buyers should choose between Non-PVC bags, PP bottles, or glass ampoules based on their specific clinical needs. Non-PVC soft bags are preferred for modern medical use due to their environmental safety and self-collapsing properties which eliminate the need for vented IV sets. Ensure the packaging features a dual-port design (one for injection, one for infusion) and maintains a high moisture barrier to prevent concentration changes during storage.

How can buyers verify the sterility and pyrogen-free quality of the product?

Request a Certificate of Analysis (COA) for every batch, specifically checking for Bacterial Endotoxins Test (BET) results and Sterility Test compliance. The product must be non-pyrogenic and isotonic. High-quality manufacturers utilize Terminal Sterilization (usually via pressurized steam at 121°C) to ensure a Sterility Assurance Level (SAL) of 10^-6.

What are the storage and shelf-life considerations for bulk procurement?

Standard 0.9% Saline typically has a shelf life of 24 to 36 months. It should be stored at controlled room temperature (20°C to 25°C). When sourcing, ensure the remaining shelf life upon arrival is at least 80% of the total duration to allow for distribution and inventory turnover. Avoid exposure to excessive heat or freezing, as this can compromise the container integrity.

Cross-Border Procurement Risks and Strategic Advice

What are the primary regulatory risks when importing medical fluids?

Medical fluids are highly regulated. The biggest risk is customs seizure due to lack of Import Licenses or Medical Device/Drug Registration in the destination country. Always verify that the supplier is registered on Made-in-China.com as a verified manufacturer and consult with a local customs broker to confirm the specific HS Code (typically 3004.90) requirements for your region.

How should shipping and logistics be managed for heavy liquid cargo?

Sodium Chloride injections are heavy and have low value-to-weight ratios. Sea freight (FCL - Full Container Load) is the most economical method. Ensure the use of heavy-duty pallets and shrink-wrapping to prevent leakage or box collapse during transit. It is critical to purchase Marine Cargo Insurance that covers 'leakage and breakage' specifically for liquid medical supplies.

What strategies can be used for price negotiation and transaction security?

Negotiate based on volume tiers; prices for 500ml bags can drop significantly when ordering in 20ft container increments. For transaction security, use Escrow services or Letters of Credit (L/C) to ensure payment is only released upon verification of the Bill of Lading and Third-party Inspection Reports (such as SGS or Intertek) confirming the batch numbers match the COA.

How to handle supplier audits for pharmaceutical products?

Before a large-scale contract, conduct a Virtual Factory Audit or hire a local agent to verify the cleanroom classification (Class 100/ISO 5 areas). Check the supplier's track record on Made-in-China.com, focusing on their export history to highly regulated markets, which serves as a proxy for their quality management maturity.

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