About Shandong Bouliga Biotechnology Co., Ltd. - Chemicals & Allied Products Supplier in China

China‑based Shandong Bouliga Biotechnology Co., Ltd. lists five active products in its catalogue, all related to hyaluronic acid. The portfolio includes a 1 ml hyaluronic acid dermal filler for facial applications, a broader line of dermal filler volumes (1 ml, 2 ml, 5 ml, 10 ml), and two powder formats identified as sodium hyaluronate with the CAS number 9004‑61‑9. Each entry falls under the “Chemicals & Allied Products” category, reflecting the company’s focus on cosmetic‑medical and raw‑material chemicals. The catalogue does not provide additional product specifications such as molecular weight or purity percentages.

The listed items are presented as sterile injectable fillers and bulk sodium hyaluronate powders. The filler products are described by their delivery volume, while the powders are identified by chemical name and CAS registration. No further manufacturing details, regulatory approvals, or third‑party certifications are supplied in the source data. The supplier’s trust tier is recorded as “harbor,” indicating a moderate level of verification within the platform.

Product Range and Specialties of Shandong Bouliga Biotechnology Co., Ltd.

The hyaluronic acid dermal fillers are supplied in sealed vials of 1 ml, 2 ml, 5 ml and 10 ml, a packaging format commonly used for aesthetic medicine. In the broader market, pharmaceutical‑grade hyaluronic acid typically meets a purity of ≥99 % and is supplied with a defined molecular weight range, often 0.5 - 2 MDa for soft‑tissue augmentation. Cosmetic‑grade powders may have purity levels of 95 - 98 % and are sold in bulk bags ranging from 25 kg to 100 kg. Sodium hyaluronate powder with CAS 9004‑61‑9 is a standard raw material for both topical formulations and injectable preparations; industry specifications frequently require moisture content below 5 % and a pH-adjusted aqueous solution for reconstitution.

Trade and Export Information - Shandong Bouliga Biotechnology Co., Ltd.

Exporters of hyaluronic acid and sodium hyaluronate from China generally target the United States, European Union, Japan and South Korea, where demand for aesthetic‑medicine products and dermal‑care ingredients is high. The products are classified under HS Chapter 29 for organic chemicals, and shipments are typically subject to documentation such as a Certificate of Origin, a Material Safety Data Sheet (MSDS) and, when destined for medical use, a declaration of compliance with GMP or ISO 13485 standards. Buyers often request third‑party laboratory analysis reports confirming purity, molecular weight distribution and endotoxin levels. Common Incoterms for these shipments are FOB Shanghai or CIF destination port, with temperature‑controlled containers used for the injectable fillers to maintain sterility.

Sourcing from Shandong Bouliga Biotechnology Co., Ltd. - Buyer Guidance

When evaluating Shandong Bouliga Biotechnology’s hyaluronic acid items, buyers should request a Certificate of Analysis that details purity, moisture content and molecular weight range. For the injectable fillers, a sterility test report and an endotoxin limit statement (e.g., <0.5 EU/mL) are typical prerequisites before acceptance. Confirm that the powder specifications match the intended formulation - verify CAS number, bulk packaging weight and any declared pH adjustment. Buyers are advised to clarify the minimum order quantity, lead time for sterile vial production and the availability of a pre‑shipment inspection report.

What forms of hyaluronic acid does the supplier offer?

The catalogue lists sterile injectable dermal fillers in 1 ml, 2 ml, 5 ml and 10 ml vials, and bulk sodium hyaluronate powder identified by CAS 9004‑61‑9.

Are the powder products suitable for medical use?

Sodium hyaluronate powder can be used for medical formulations, but buyers should obtain a GMP or ISO 13485 compliance certificate and a purity ≥ 99 % analysis before use.

What documentation should a buyer request before placing an order?

A Certificate of Analysis, Material Safety Data Sheet, sterility test report for injectables, and a declaration of compliance with relevant quality standards are standard documents.

Is there a typical minimum order quantity for the powder?

Bulk sodium hyaluronate is usually supplied in 25 kg or 100 kg bags; the exact MOQ should be confirmed with the supplier.

What packaging is used for the dermal filler vials?

The filler is supplied in sealed glass or polymer vials pre‑filled with 1 ml, 2 ml, 5 ml or 10 ml of sterile solution, often packed in insulated cartons for temperature control.

Which certifications are commonly required for importing these products?

Importers typically require GMP, ISO 13485, and, for EU markets, CE marking or a conformity assessment for medical devices, together with a valid Certificate of Origin.

What shipping terms are most frequently used for these goods?

Suppliers from China often ship under FOB Shanghai or CIF destination port, using temperature‑controlled containers for the injectable products.

How can a buyer verify the product’s molecular weight?

The Certificate of Analysis should include the molecular weight distribution, commonly expressed in Daltons (e.g., 0.5 - 2 MDa for cosmetic grade).