← Back to catalogue

Augments

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 96-0866Model PFC Sigma Augments

by DePuy Ireland UC

Identity

Trade Name
P.F.C. SIGMA FDA UDI
Generic Name
Knee arthroplasty wedge FDA UDI
Device Name
Augments EUDAMED
P.F.C. SIGMA POSTERIOR AUGMENT COMBO CEMENTED SIZE 3 4mm FDA UDI
Model / Reference
PFC Sigma Augments EUDAMED
96-0866 EUDAMEDFDA UDI
Description
P.F.C. SIGMA POSTERIOR AUGMENT COMBO CEMENTED SIZE 3 4mm FDA UDI

Identifiers

Catalog Number
960866 FDA UDI
Primary DI / UDI-DI
10603295234302 EUDAMEDFDA UDI
Basic UDI-DI
0603295a004408N EUDAMED
FDA Product Code
NJL FDA UDI
JWH FDA UDI
EMDN Code
P09098001 KNEE PROSTHESES AUGMENTS EUDAMED
GMDN Term
Knee arthroplasty wedge FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class III FDA UDI
Regulation Number
888.3560 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Augments by DePuy Ireland UC — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
DePuy Ireland UC
EUDAMED SRN
IE-MF-000007377

Sources (2)

  • EUDAMED 52449f4c-e75b-4ced-ac60-7a7a641b294d 61 fields · synced Jun 19, 2026
  • FDA UDI 747557b2-1487-43d1-ba99-58f7833bc1db 35 fields · synced May 30, 2026