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Physica

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
PHYSICA FDA UDI
Generic Name
Polyethylene patella prosthesis FDA UDI
Device Name
Patellar prosthesis dia. 41mm FDA UDI
Model / Reference
Patellar Prosthesis FDA UDI
Description
Patellar prosthesis dia. 41mm FDA UDI

Identifiers

Catalog Number
6595.50.041 FDA UDI
Primary DI / UDI-DI
08033390091046 FDA UDI
510(k) Number
K141934 FDA UDI
FDA Product Code
HRY FDA UDI
JWH FDA UDI
GMDN Term
Polyethylene patella prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3530 FDA UDI
888.3560 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: Polyethylene patella prosthesis

Physica by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyethylene patella prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI dd28114a-a084-4cbf-bd16-21c8ec50af74 36 fields · synced Jun 8, 2026