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Sigma

FDA UDI

Class III (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
SIGMA FDA UDI
Generic Name
Uncoated knee femur prosthesis, metallic FDA UDI
Device Name
SIGMA FEMORAL POSTERIOR STABILIZED LUGGED CEMENTED SIZE 3 RIGHT FDA UDI
Model / Reference
1960-73-500 FDA UDI
Description
SIGMA FEMORAL POSTERIOR STABILIZED LUGGED CEMENTED SIZE 3 RIGHT FDA UDI

Identifiers

Catalog Number
196073500 FDA UDI
Primary DI / UDI-DI
10603295075479 FDA UDI
FDA Product Code
NJL FDA UDI
JWH FDA UDI
GMDN Term
Uncoated knee femur prosthesis, metallic 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

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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Uncoated knee femur prosthesis, metallic

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

Similar devices

Also classified as Uncoated knee femur prosthesis, metallic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 6b9470e5-3b9c-4ec5-b2d4-30db52957ea8 35 fields · synced Jun 1, 2026