← Back to catalogue

Extremities Instrumentsbanalec Bone Holding Forceps - Curved, Left

FDA UDI

Class I (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
EXTREMITIES INSTRUMENTSBANALEC BONE HOLDING FORCEPS - CURVED, LEFT FDA UDI
Generic Name
Implant handling forceps, scissors-like FDA UDI
Model / Reference
PF541 FDA UDI

Identifiers

Catalog Number
PF541 FDA UDI
Primary DI / UDI-DI
00887868118289 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Implant handling forceps, scissors-like FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: Implant handling forceps, scissors-like

Extremities Instrumentsbanalec Bone Holding Forceps - Curved, Left by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Implant handling forceps, scissors-like.

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

Sources (1)

  • FDA UDI 2a42cbb6-d653-41b6-a71b-20d66988269c 34 fields · synced May 30, 2026