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Perfecta

FDA UDI

Class III (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 IMC II STANDARD COLLARED SIZE 16.5 FDA UDI
Model / Reference
39081650 FDA UDI
Description
PERFECTA IMC II STANDARD COLLARED SIZE 16.5 FDA UDI

Identifiers

Catalog Number
39081650 FDA UDI
Primary DI / UDI-DI
M684390816501 FDA UDI
FDA Product Code
MRA FDA UDI
JDI FDA UDI
LPH FDA UDI
GMDN Term
Uncoated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
888.3350 FDA UDI
888.3358 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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 16.5 Millimeter FDA UDI

Category: Uncoated femoral stem prosthesis, modular

Perfecta by MicroPort Orthopedics Inc. — Class III — 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 18c67e58-3c3d-45f9-9686-25d7c2e2cb5c 36 fields · synced Jun 9, 2026