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Biomet®

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
Biomet® FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Model / Reference
010001038 FDA UDI

Identifiers

Catalog Number
010001038 FDA UDI
Primary DI / UDI-DI
00880304527850 FDA UDI
510(k) Number
K121874 FDA UDI
FDA Product Code
OQG FDA UDI
LZO FDA UDI
OQI FDA UDI
LPH FDA UDI
PBI FDA UDI
OQH FDA UDI
JDI FDA UDI
LWZ FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 FDA UDI
888.3310 FDA UDI
888.3350 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

Yes

FDA UDI

Category: Metallic femoral head prosthesis

Biomet® by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

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 f4383ef5-233c-4abe-b2be-3feee2d5eb0c 36 fields · synced May 30, 2026