Sodium lactate ringer
I have found results from300+products and90+suppliers aboutSodium lactate ringer
Sodium Lactate Ringer Injection 500ml Finished Medicines with GMP
Premium Sodium Lactate Ringer Solution 500ml with GMP Certification
Premium Sodium Lactate Ringer Injection Solution 500ml Pack
Large Volume Sodium Lactate Ringer IV Injection 500ml
High-Quality Sodium Lactate Ringer Solution 500ml for Nutritional Support
Huaren Pharmaceuticals/Sodium Lactate Ringer’ S Injection
CMP Certified Sodium Lactate Ringer's Injection 500ml-Huaren Pharmaceutical
Top Quality Sodium Lactate Ringer Injection 500ml CMP Certified -Huaren Pharmaceutical
High Quality GMP Certified Medicine 500ml Sodium Lactate Ringer's Injection-Huaren Pharmaceutical
Electrolytes GMP Certificate High Quality OEM Lactate Ringer Injection USP 500ml
Supply Sodium Lactate Ringer's Injection 500ml for IV Therapy
Ringer Lactate Injection/Sodium Ringer Lactate for Injection
Ringer Lactate Injection Medicine Infusion 500ml
Ringer Lactate Injection Medicine Infusion 500ml
Ringer Lactate Injection/Sodium Ringer Lactate for Injection
GMP Sodium Lactate Ringer Injection with 500ml 1bottle/ Box
Pharmaceutical Distributor Sodium Lactate Ringer’ S Injection 500ml
Sodium Lactate Ringer's Injection Large Volume Intravenous Solution (IV) for Infusion, USP (Ringer)
Sodium Lactate Ringer′ S Injection / Lactated Ringer′ S Injection
Sourcing guidance for Sodium Lactate Ringer
What are the key technical specifications and quality standards for Sodium Lactate Ringer?
Sodium Lactate Ringer is a critical pharmaceutical product that must adhere to Pharmacopoeia standards (USP, BP, or EP). Key specifications include a precise electrolyte balance: Sodium (130 mEq/L), Potassium (4 mEq/L), Calcium (2.7-3 mEq/L), and Lactate (28 mEq/L). The solution must be pyrogen-free, sterile, and have a pH range between 6.0 and 7.5. Buyers should verify the osmolarity (approx. 273 mOsm/L) to ensure it is isotonic and safe for intravenous administration.
What certifications should a professional B2B buyer verify before purchasing?
Suppliers must possess a valid GMP (Good Manufacturing Practice) certificate to ensure the production environment meets medical standards. Additionally, look for ISO 13485 (Medical Devices Quality Management) and CE marking or FDA approval depending on the target market. For cross-border trade, a Certificate of Analysis (COA) for every batch and a Free Sale Certificate (FSC) are mandatory to facilitate customs clearance and clinical use.
How should the packaging and container material be evaluated for safety?
The solution is typically packaged in PVC-free bags, PP bottles, or glass bottles. B2B buyers should prioritize non-PVC and DEHP-free materials to prevent chemical leaching into the fluid. Ensure the packaging features a self-sealing injection port and clear graduations. For long-distance shipping, the outer cartons must be moisture-proof and reinforced to prevent leakage or contamination during transit.
What are the primary usage scenarios and clinical functions of this product?
It is primarily used for fluid resuscitation after blood loss or trauma, treating metabolic acidosis, and providing electrolyte replacement. Unlike normal saline, it is preferred in surgical settings because the lactate is metabolized into bicarbonate by the liver, helping to maintain acid-base balance. It is a staple for hospitals, emergency medical services, and veterinary clinics.
Cross-Border Procurement & Risk Management for Medical Fluids
What are the specific logistics and storage requirements for international shipping?
Sodium Lactate Ringer is heavy and sensitive to temperature extremes. It should be stored and transported between 15°C to 30°C (59°F to 86°F). Avoid freezing, as this can damage the container integrity. Buyers should use reefer containers if transiting through extreme climates and ensure the freight forwarder is experienced in cold chain or medical-grade logistics.
How can buyers mitigate risks when sourcing from overseas suppliers?
Utilize Made-in-China.com’s Secured Trading services to protect your payment until delivery is confirmed. Conduct a factory audit (either in-person or via a third-party like SGS/TÜV) to verify the supplier's actual production capacity and sterile room conditions. Always request a pre-shipment inspection to verify batch numbers and expiration dates (which should ideally be 24-36 months from the date of manufacture).
What are the common customs and regulatory hurdles in cross-border medical trade?
Medical fluids are highly regulated. You must ensure the product's HS Code (typically 3004.90) is correctly classified. The importer must often have a Medical Device/Pharmaceutical Import License in their home country. Failure to provide a Material Safety Data Sheet (MSDS) or the correct Product Registration Certificate can lead to immediate seizure by customs.
What strategies should be used for price negotiation with medical manufacturers?
Focus on volume-based pricing; because the margins on IV fluids are thin, significant discounts are usually only available for Full Container Load (FCL) orders. Negotiate based on packaging durability and shelf-life guarantees rather than just the unit price. A supplier offering a longer shelf life provides better economic value by reducing the risk of inventory expiration.





























