Birmingham Hip Resurfacing(bhr)

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: BIRMINGHAM HIP RESURFACING(BHR) FDA UDI
Generic Name: Femoral head prosthesis trial FDA UDI
Device Name: MODULAR HEAD TRIAL 58MM FDA UDI
Model / Reference: 90035558 FDA UDI
Description: MODULAR HEAD TRIAL 58MM FDA UDI

Identifiers

Catalog Number: 90035558 FDA UDI
Primary DI / UDI-DI: 03596010578617 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Femoral head prosthesis trial 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Femoral head prosthesis trial

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

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Also classified as Femoral head prosthesis trial.

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Klassic Femoral Head Trial — TOTAL JOINT ORTHOPEDICS, INC. · Class I
AcuMatch — Exactech, Inc. · Class I
G7® — Biomet Orthopedics, Inc. · Class II
AcuMatch — Exactech, Inc. · Class I
NovoHip Total Hip System — Novosource, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI 6ac05eb9-c49d-4f04-99e6-78bcd78da2d4 35 fields · synced Jun 8, 2026