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Birmingham Hip Resurfacing (bhr)

FDA UDI

Class III (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
BIRMINGHAM HIP RESURFACING (BHR) FDA UDI
Generic Name
Orthopaedic implant impactor, reusable FDA UDI
Device Name
DYSPLASIA CUP HAP 52/60 FDA UDI
Model / Reference
74122260 FDA UDI
Description
DYSPLASIA CUP HAP 52/60 FDA UDI

Identifiers

Catalog Number
74122260 FDA UDI
Primary DI / UDI-DI
03596010552389 FDA UDI
PMA Number
P040033 FDA UDI
FDA Product Code
NXT FDA UDI
GMDN Term
Orthopaedic implant impactor, reusable FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic implant impactor, reusable

Birmingham Hip Resurfacing (bhr) by Smith & Nephew, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant impactor, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5197c6fc-7569-490e-a91b-496f94e769f2 36 fields · synced Jun 8, 2026