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MULTIGEN PLUS Knee Instrument Set

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
MULTIGEN PLUS Knee Instrument Set FDA UDI
Generic Name
Patella prosthesis trial FDA UDI
Device Name
Trial Patellar Dome-Dia.=32mm h8mm FDA UDI
Model / Reference
Trial Patellar Dome FDA UDI
Description
Trial Patellar Dome-Dia.=32mm h8mm FDA UDI

Identifiers

Catalog Number
9066.40.132 FDA UDI
Primary DI / UDI-DI
08033390036207 FDA UDI
510(k) Number
K141934 FDA UDI
FDA Product Code
HRY FDA UDI
JWH FDA UDI
GMDN Term
Patella prosthesis trial 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: Patella prosthesis trial

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

Similar devices

Also classified as Patella prosthesis trial.

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 4a9780a3-e557-49fd-8a83-295e5cbceac3 36 fields · synced Jun 8, 2026