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Physica Ps

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
PHYSICA PS FDA UDI
Generic Name
Knee femur prosthesis trial, reusable FDA UDI
Device Name
#1-Right-Trial Femoral Component FDA UDI
Model / Reference
Trial Femoral Component FDA UDI
Description
#1-Right-Trial Femoral Component FDA UDI

Identifiers

Catalog Number
9065.15.110 FDA UDI
Primary DI / UDI-DI
08033390096379 FDA UDI
510(k) Number
K152008 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Knee femur prosthesis trial, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Knee femur prosthesis trial, reusable

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

Similar devices

Also classified as Knee femur prosthesis trial, reusable.

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 c3190abd-5408-4183-b6f6-d0e22720bfa8 36 fields · synced May 31, 2026