← Back to catalogue

Fassier-Duval Telescopic Im System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref G-WIRE 018Model GUIDE WIRE

by Orthopediatrics Canada ULC

Identity

Trade Name
The Fassier-Duval Telescopic IM System EUDAMED
FASSIER-DUVAL TELESCOPIC IM SYSTEM FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
FD GUIDE WIRE Ø1.8mm X 457mm FDA UDI
Model / Reference
G-WIRE 018 EUDAMEDFDA UDI
GUIDE WIRE EUDAMED
Description
FD GUIDE WIRE Ø1.8mm X 457mm FDA UDI

Identifiers

Catalog Number
G-WIRE 018 FDA UDI
Primary DI / UDI-DI
07540194014962 EUDAMEDFDA UDI
Basic UDI-DI
7540194FD-GWR9 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
Z12139085 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Orthopaedic guidewire, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

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

Dimensions & Sizes

Size
Length — 457 Millimeter FDA UDI
Outer Diameter — 1.8 Millimeter FDA UDI

Category: Orthopaedic guidewire, single-use

Fassier-Duval Telescopic Im System by Orthopediatrics Canada ULC — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI f08b533c-c968-4f6f-bfe9-0bea85715467 37 fields · synced Jun 19, 2026
  • EUDAMED 3646c568-70a9-4e41-8825-e576f7ca2d18 61 fields · synced Jun 19, 2026