← Back to catalogue

Hip Instrumentationasi Straight Offset Rasp Handle

FDA UDI

Class I (US FDA UDI)

by Biomet Uk Ltd

Identity

Trade Name
HIP INSTRUMENTATIONASI STRAIGHT OFFSET RASP HANDLE FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Model / Reference
110017521 FDA UDI

Identifiers

Catalog Number
110017521 FDA UDI
Primary DI / UDI-DI
05019279935475 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting 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: Surgical instrument handle, non-torque-limiting

Hip Instrumentationasi Straight Offset Rasp Handle by Biomet Uk Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

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
Biomet Uk Ltd

Sources (1)

  • FDA UDI 78fd2245-10b7-4a60-b59a-e2d4854a3924 34 fields · synced May 30, 2026