← Back to catalogue

Fassier-Duval Telescopic Im System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref FTRP109Model FEMALE TREPHINE

by Orthopediatrics Canada ULC

Identity

Trade Name
The Fassier-Duval Telescopic IM System EUDAMED
FASSIER-DUVAL TELESCOPIC IM SYSTEM FDA UDI
Generic Name
Bone trephine, reusable FDA UDI
Device Name
FEMALE TREPHINE 9.0MM FDA UDI
Model / Reference
FTRP109 EUDAMEDFDA UDI
FEMALE TREPHINE EUDAMED
Description
FEMALE TREPHINE 9.0MM FDA UDI

Identifiers

Catalog Number
FTRP109 FDA UDI
Primary DI / UDI-DI
07540194013019 EUDAMEDFDA UDI
Basic UDI-DI
7540194FD-FTRLX EUDAMED
FDA Product Code
HWK FDA UDI
EMDN Code
L090902 ORTHOPAEDIC SURGERY TREPHINES, REUSABLE EUDAMED
GMDN Term
Bone trephine, reusable 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

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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
Outer Diameter — 9.10 Millimeter FDA UDI

Category: Bone trephine, reusable

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 Bone trephine, reusable.

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 962e0387-59b2-4a90-9a0a-81407c8a870a 36 fields · synced Jun 19, 2026
  • EUDAMED 716b2bb3-0515-442f-b022-5c11e7b9fa0e 61 fields · synced Jun 19, 2026