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Supartz

FDA UDI

Class III (US FDA UDI)

by Acre Pharma Limited

Identity

Trade Name
Supartz FDA UDI
Generic Name
Synovial fluid supplementation medium FDA UDI
Device Name
Injected into the knee to relieve the pain from osteoarthritis. FDA UDI
Model / Reference
NA FDA UDI
Description
Injected into the knee to relieve the pain from osteoarthritis. FDA UDI

Identifiers

Primary DI / UDI-DI
05060604130027 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 Acre Pharma Limited — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synovial fluid supplementation medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acre Pharma Limited

Sources (1)

  • FDA UDI 4a158b05-28dc-4ffa-b8b1-6f7fd9e2111b 34 fields · synced May 30, 2026