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MULTIGEN PLUS Knee

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
MULTIGEN PLUS Knee FDA UDI
Generic Name
Surgical flat-nosed pliers FDA UDI
Device Name
Tibial Nail Extractor Plier FDA UDI
Model / Reference
Tibial Nail Extractor Plier FDA UDI
Description
Tibial Nail Extractor Plier FDA UDI

Identifiers

Catalog Number
9066.22.180 FDA UDI
Primary DI / UDI-DI
08033390056809 FDA UDI
510(k) Number
K141934 FDA UDI
FDA Product Code
HRY FDA UDI
JWH FDA UDI
GMDN Term
Surgical flat-nosed pliers 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: Surgical flat-nosed pliers

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

Similar devices

Also classified as Surgical flat-nosed pliers.

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 67ba7a71-18d2-4b3a-8b92-0fe44d0bcf4a 35 fields · synced May 30, 2026