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Sodium Hyaluronate Filler in The Osteoarthritis and Rheumatoid Arthritis

China Sodium Hyaluronate Filler in The Osteoarthritis and Rheumatoid Arthritis, Find details about China Hyaluronate Filler in The Osteoarthritis, Hyaluronic Acid Gel from Sodium Hyaluronate Filler in The Osteoarthritis and Rheumatoid Arthritis

Model NO.
2ml 3ml 5ml
Appearance
Colorless
Hyaluronate Content
22mg/Ml
pH
6.5~7.5
Osmotic Pressure (Mosmol/L)
270-350
Swelling Degree
Less 20
Trademark
Meibonda
Transport Package
Injector
Specification
CE, ISO, GMP
Origin
Shandong China
HS Code
3913900000
Model NO.
2ml 3ml 5ml
Appearance
Colorless
Hyaluronate Content
22mg/Ml
pH
6.5~7.5
Osmotic Pressure (Mosmol/L)
270-350
Swelling Degree
Less 20
Trademark
Meibonda
Transport Package
Injector
Specification
CE, ISO, GMP
Origin
Shandong China
HS Code
3913900000
 Sodium Hyaluronate Filler in The Osteoarthritis and Rheumatoid Arthritis
Performance:
1. Preparation component: Sodium hyaluronate1%
2. Preparation performance: No color, no smeel and high transparent sticky liquid; PH: 6.8~7.5
3. Fine consistency
4. Dynamic viscosity≥ 10000mpas
Sodium Hyaluronate Filler in The Osteoarthritis and Rheumatoid Arthritis
Application range:
Traumatic arthritis
Osteoarthritis (rheumatoid arthritis)
RA (rheumatoid arthritis)
Scapulohumeral per arthritis
Tendon repair
Arthroscopic surgery
Adhesion of soft issues
Joint inspection
Degenerative arthritis
Per arthritis of shoulder joint

Dosage:
Anterior chamber injection amount should be less than 1ml and posterior chamber injection amount should be less than 2ml.

Storage: 2-8 Celsius to avoid freezing and direct light
Period of validity: 2 years
Specifications: 1.0ml/piece. 1.5ml/piece 2.0ml/piece.
Sodium Hyaluronate Filler in The Osteoarthritis and Rheumatoid Arthritis

Test  Items
Standard Provision
Result

Appearance
Colorless,transparent No visible foreign matter, no air bubbles.
Qualified

Hyaluronate Content
2 2 ± 3mg/ml
23 mg/ml

PH
6.5~7.5
6.56

Osmotic Pressure( mOsmol/L )
270_ 350
312

P article size distribution (μ m )
< 400
Qualified

Swelling degree
< 20
13.9

Crosslinking agent  BDDE  residue (μ g/g )
≤ 2.0
1.48

P rotein
≤ 0.1%
Qualified

H eavy metal
≤ 20ppm
Qualified

Bacteria Test
S houle have no bacterial
Qualified

Bacteria Endotoxin Test
≤ 0.5EU/mL
Qualified

H emolytic
Should be no hemolysis ring
Qualified

Conclusion
Conclusion: The produces were tested conform to the standard of  Enterprise  Standard,Qualified

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