P.f.c. Sigma

FDA UDI

Class III (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name: P.F.C. SIGMA FDA UDI
Generic Name: Knee femur stem prosthesis FDA UDI
Device Name: P.F.C. SIGMA FLUTED FEMORAL STEM 16mm x 125mm 5 DEGREE FDA UDI
Model / Reference: 96-0702 FDA UDI
Description: P.F.C. SIGMA FLUTED FEMORAL STEM 16mm x 125mm 5 DEGREE FDA UDI

Identifiers

Catalog Number: 960702 FDA UDI
Primary DI / UDI-DI: 10603295233633 FDA UDI
FDA Product Code: NJL FDA UDI
JWH FDA UDI
GMDN Term: Knee femur stem prosthesis FDA UDI

Classification

Device Class: Class III FDA UDI
Regulation Number: 888.3560 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

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Knee femur stem prosthesis

P.f.c. Sigma by Depuy (ireland) — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee femur stem prosthesis.

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LINK Endo-Model EVO — WALDEMAR LINK GmbH & Co. KG · Class II
OPTILOCK PERIARTICULAR PLATING SYSTEM — Biomet Orthopedics, Inc. · Class II
Evolution Revision CCK System — MicroPort Orthopedics Inc. · Class II
Modular Stem, — WALDEMAR LINK GmbH & Co. KG · Class II
LINK Endo-Model EVO Knee System — WALDEMAR LINK GmbH & Co. KG · 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: Depuy (ireland)

Sources (1)

FDA UDI b75dd70a-ec9f-4fde-b4b3-00dc8e94ee4f 35 fields · synced May 30, 2026