← Back to catalogue

PHYSICA Instrument Set

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
PHYSICA Instrument Set FDA UDI
Generic Name
Knee tibia prosthesis trial, reusable FDA UDI
Device Name
KR Trial Liner #9 - H.20mm - Right FDA UDI
Model / Reference
KR Trial Liner FDA UDI
Description
KR Trial Liner #9 - H.20mm - Right FDA UDI

Identifiers

Catalog Number
9065.31.920 FDA UDI
Primary DI / UDI-DI
08033390093002 FDA UDI
510(k) Number
K141934 FDA UDI
FDA Product Code
HRY FDA UDI
JWH FDA UDI
GMDN Term
Knee tibia prosthesis trial, reusable 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

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 tibia prosthesis trial, reusable

PHYSICA Instrument Set by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee tibia prosthesis trial, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 951456c7-a374-4d46-8125-85423a50fe7d 36 fields · synced May 30, 2026