Perfecta

FDA UDI

Class III (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name: Perfecta FDA UDI
Generic Name: Press-fit hip femur prosthesis, modular FDA UDI
Device Name: PERFECTA RS II REDUCED FLARE COLLARLESS SIZE 12.7 FDA UDI
Model / Reference: 39001270 FDA UDI
Description: PERFECTA RS II REDUCED FLARE COLLARLESS SIZE 12.7 FDA UDI

Identifiers

Catalog Number: 39001270 FDA UDI
Primary DI / UDI-DI: M684390012701 FDA UDI
FDA Product Code: MRA FDA UDI
JDI FDA UDI
LPH FDA UDI
GMDN Term: Press-fit hip femur 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 12.7 Millimeter FDA UDI

Category: Press-fit hip femur prosthesis, modular

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

Similar devices

Also classified as Press-fit hip femur prosthesis, modular.

Alloclassic® Zweymüller® — Zimmer, Inc. · Class II
Wagner SL Revision® — Zimmer, Inc. · Class II
VerSys® — Zimmer, Inc. · Class II
Wagner Cone Prosthesis® — Zimmer, Inc. · Class II
SUMMIT — DEPUY ORTHOPAEDICS, INC. · Class II
Alloclassic® Zweymüller® — Zimmer, Inc. · Class II
UniSyn Hip System — SHALBY ADVANCED TECHNOLOGIES, INC. · Class II
VerSys® — Zimmer, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: MicroPort Orthopedics Inc.

Sources (1)

FDA UDI 51f70df7-fe9c-497c-bbd5-ec1ec0a77c5e 36 fields · synced Jun 9, 2026