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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 acetabulum prosthesis FDA UDI
Device Name
PLASMA SPRAYED FINNED SOLID ACETABULAR SHELL 60-61mm OD FDA UDI
Model / Reference
3672006000 FDA UDI
Description
PLASMA SPRAYED FINNED SOLID ACETABULAR SHELL 60-61mm OD FDA UDI

Identifiers

Catalog Number
3672006000 FDA UDI
Primary DI / UDI-DI
M68436720060001 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Metallic acetabulum prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Dimensions & Sizes

Size
Outer Diameter — 60 Millimeter FDA UDI

Category: Metallic acetabulum prosthesis

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

Similar devices

Also classified as Metallic acetabulum prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afc77392-605a-45db-9bfb-a3d2e9169f63 36 fields · synced Jun 9, 2026