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Plif Sg Instruments

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 273130001Model PLIF SG Orthopaedic surgery, Cutting Instruments- Others

by Medos International SARL

Identity

Trade Name
PLIF SG INSTRUMENTS EUDAMED
PLIF FDA UDI
Generic Name
Orthopaedic knife FDA UDI
Device Name
PLIF SG Knife EUDAMED
PLIF SG INSTRUMENTS GANGLION KNIFE (SLIM JIM JR.) FDA UDI
Model / Reference
PLIF SG Orthopaedic surgery, Cutting Instruments- Others EUDAMED
273130001 EUDAMEDFDA UDI
Description
PLIF SG INSTRUMENTS GANGLION KNIFE (SLIM JIM JR.) FDA UDI

Identifiers

Catalog Number
273130001 FDA UDI
Primary DI / UDI-DI
10705034187006 EUDAMEDFDA UDI
Basic UDI-DI
0705034a000565X EUDAMED
Direct Marketing DI
10705034187006 EUDAMED
FDA Product Code
HTS FDA UDI
EMDN Code
L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic knife FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone cutting forceps, reusable

Plif Sg Instruments by Medos International Sarl — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutting forceps, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CH-MF-000014268
Authorised Representative
DePuy Ireland UC IE-AR-000009328

Sources (2)

  • EUDAMED 24e04198-e710-40f9-a5d5-1bd34b3fadc5 61 fields · synced Jul 26, 2026
  • FDA UDI fb059ebd-cd66-4dad-b8ef-478d97a3790a 35 fields · synced May 30, 2026