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Fassier-Duval Telescopic Im System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref MR248-SModel COIL PULLER

by Orthopediatrics Canada ULC

Identity

Trade Name
The Fassier-Duval Telescopic IM System EUDAMED
FASSIER-DUVAL TELESCOPIC IM SYSTEM FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, single-use FDA UDI
Device Name
COIL-PULLER SHAFT Ø4.8mm FDA UDI
Model / Reference
MR248-S EUDAMEDFDA UDI
COIL PULLER EUDAMED
Description
COIL-PULLER SHAFT Ø4.8mm FDA UDI

Identifiers

Catalog Number
MR248-S FDA UDI
Primary DI / UDI-DI
07540194007568 EUDAMEDFDA UDI
Basic UDI-DI
7540194FD-CPSL6 EUDAMED
FDA Product Code
HWB FDA UDI
EMDN Code
Z12139085 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Orthopaedic inorganic implant inserter/extractor, 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
Lumen/Inner Diameter — 3.28 Millimeter FDA UDI

Category: Orthopaedic inorganic implant inserter/extractor, 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 inorganic implant inserter/extractor, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 268b7ea2-c282-4cce-96f5-832175659d43 37 fields · synced Jun 18, 2026
  • EUDAMED 2fedbc64-6e07-4bb2-8415-8686004b643b 61 fields · synced Jun 18, 2026