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MULTIGEN Knee

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
MULTIGEN Knee FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
Patellar Gauge FDA UDI
Model / Reference
Patellar Gauge FDA UDI
Description
Patellar Gauge FDA UDI

Identifiers

Catalog Number
9066.40.050 FDA UDI
Primary DI / UDI-DI
08033390114806 FDA UDI
510(k) Number
K141934 FDA UDI
FDA Product Code
JWH FDA UDI
HRY FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
888.3530 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: Surgical implant template, reusable

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

Similar devices

Also classified as Surgical implant template, 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 489cc894-c464-43a9-b7d3-9d3cdcc307c5 35 fields · synced May 30, 2026