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Supartz

FDA UDI

Class III (US FDA UDI)

by Pavan Trading Ltd

Identity

Trade Name
Supartz FDA UDI
Generic Name
Synovial fluid supplementation medium FDA UDI
Device Name
Supartz is injected into the knee to relieve the pain of osteoarthritis. FDA UDI
Model / Reference
None FDA UDI
Description
Supartz is injected into the knee to relieve the pain of osteoarthritis. FDA UDI

Identifiers

Primary DI / UDI-DI
05060548950057 FDA UDI
PMA Number
P980044 FDA UDI
FDA Product Code
MOZ FDA UDI
GMDN Term
Synovial fluid supplementation medium FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synovial fluid supplementation medium

Supartz by Pavan Trading Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synovial fluid supplementation medium.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pavan Trading Ltd

Sources (1)

  • FDA UDI ae856450-8bc9-498b-a59a-1571350c7c89 34 fields · synced Jun 8, 2026