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Perfecta

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Perfecta FDA UDI
Generic Name
Uncoated femoral stem prosthesis, modular FDA UDI
Device Name
PERFECTA® RA COCR POLISHED HIP SIZE 16.5 SLT TAPER COLLARLESS FDA UDI
Model / Reference
37561650 FDA UDI
Description
PERFECTA® RA COCR POLISHED HIP SIZE 16.5 SLT TAPER COLLARLESS FDA UDI

Identifiers

Catalog Number
37561650 FDA UDI
Primary DI / UDI-DI
M684375616501 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Uncoated femoral stem prosthesis, modular 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

Category: Uncoated femoral stem prosthesis, modular

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

Similar devices

Also classified as Uncoated femoral stem prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MicroPort Orthopedics Inc.

Sources (1)

  • FDA UDI 61557711-5135-42ef-8459-0de6d41a368a 35 fields · synced Jun 9, 2026