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Birmingham Hip

FDA UDI

Class III (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
BIRMINGHAM HIP FDA UDI
Generic Name
Orthopaedic surgery tissue debris collector, reusable FDA UDI
Device Name
BIRMINGHAM HIP DEBRIS CAP 54MM FDA UDI
Model / Reference
90127738 FDA UDI
Description
BIRMINGHAM HIP DEBRIS CAP 54MM FDA UDI

Identifiers

Catalog Number
90127738 FDA UDI
Primary DI / UDI-DI
00885556075296 FDA UDI
PMA Number
P040033 FDA UDI
FDA Product Code
NXT FDA UDI
GMDN Term
Orthopaedic surgery tissue debris collector, reusable FDA UDI

Classification

Device Class
Class III 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: Orthopaedic surgery tissue debris collector, reusable

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

Similar devices

Also classified as Orthopaedic surgery tissue debris collector, reusable.

Cleared under the same submission

P040033 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI c61f35a0-a114-44a2-bdf6-4ace2aa4078c 36 fields · synced Jun 8, 2026