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 LATERALIZED SZ 13.5 FDA UDI
Model / Reference: 39011350 FDA UDI
Description: PERFECTA RS II REDUCED FLARE COLLARLESS LATERALIZED SZ 13.5 FDA UDI

Identifiers

Catalog Number: 39011350 FDA UDI
Primary DI / UDI-DI: M684390113501 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 — 13.5 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

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Manufacturer

Manufacturer: MicroPort Orthopedics Inc.

Sources (1)

FDA UDI a04cd0ed-14c8-4de3-96a9-3da6105da094 36 fields · synced Jun 9, 2026