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Implant Partners

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Implant Partners FDA UDI
Generic Name
Metallic acetabulum prosthesis FDA UDI
Device Name
PC SHELL 54MM GROUP E IMPLANT PARTNERS™ FDA UDI
Model / Reference
DSPCGE54WD FDA UDI
Description
PC SHELL 54MM GROUP E IMPLANT PARTNERS™ FDA UDI

Identifiers

Catalog Number
DSPCGE54WD FDA UDI
Primary DI / UDI-DI
M684DSPCGE54WD1 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Metallic acetabulum 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 — 54 Millimeter FDA UDI

Category: Metallic acetabulum prosthesis

Implant Partners 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 e8438e11-0488-44ff-99af-e2339c569f1d 36 fields · synced Jun 9, 2026