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OMNI Hip

FDA UDI

Class II (US FDA UDI)

by OMNIlife science, Inc.

Identity

Trade Name
OMNI Hip FDA UDI
Generic Name
Ceramic femoral head prosthesis FDA UDI
Device Name
Biolox Delta Femoral Head 40 mm -4mm FDA UDI
Model / Reference
H3-54099 FDA UDI
Description
Biolox Delta Femoral Head 40 mm -4mm FDA UDI

Identifiers

Catalog Number
H3-54099 FDA UDI
Primary DI / UDI-DI
00841690119340 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Ceramic femoral head prosthesis

OMNI Hip by OMNIlife science, Inc. — 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 639f29fa-e733-42ec-9d7d-16877f9d3a65 35 fields · synced Jun 9, 2026