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Biolox

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
Biolox FDA UDI
Generic Name
Ceramic femoral head prosthesis FDA UDI
Device Name
Ceramic V40 Femoral Head FDA UDI
Model / Reference
6570-0-132 FDA UDI
Description
Ceramic V40 Femoral Head FDA UDI

Identifiers

Catalog Number
6570-0-132 FDA UDI
Primary DI / UDI-DI
04546540608505 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Ceramic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 32.0 Millimeter FDA UDI

Category: Ceramic femoral head prosthesis

Biolox by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic femoral head prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8439b71f-e5ee-4191-b25f-9b4dd72896c8 35 fields · synced May 31, 2026