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Birmingham Hip

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
BIRMINGHAM HIP FDA UDI
Generic Name
Ceramic acetabular liner FDA UDI
Device Name
38/22MM BH DUAL MOBILITY INSERT FDA UDI
Model / Reference
74121638 FDA UDI
Description
38/22MM BH DUAL MOBILITY INSERT FDA UDI

Identifiers

Catalog Number
74121638 FDA UDI
Primary DI / UDI-DI
00885556577189 FDA UDI
510(k) Number
K171934 FDA UDI
K211176 FDA UDI
FDA Product Code
LPH FDA UDI
JDI FDA UDI
KWY FDA UDI
GMDN Term
Ceramic acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3350 FDA UDI
888.3390 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Ceramic acetabular liner

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

Similar devices

Also classified as Ceramic acetabular liner.

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 324d7046-10b4-4fa7-bbb3-b73b50250ebd 37 fields · synced Jun 8, 2026