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Orthomet

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Orthomet FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
OMET TAPER CoCr FEM HEAD 28mm +15mm NECK FDA UDI
Model / Reference
3611281500 FDA UDI
Description
OMET TAPER CoCr FEM HEAD 28mm +15mm NECK FDA UDI

Identifiers

Catalog Number
3611281500 FDA UDI
Primary DI / UDI-DI
M68436112815001 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Metallic 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 28 Millimeter FDA UDI

Category: Metallic femoral head prosthesis

Orthomet by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f33ec2f5-9161-4a46-a247-aa18c0d79476 36 fields · synced Jun 9, 2026