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Fassier-Duval Telescopic Im System

FDA UDI

Class II (US FDA UDI)

by Orthopediatrics Canada ULC

Identity

Trade Name
FASSIER-DUVAL TELESCOPIC IM SYSTEM FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
Male Long Component for Ø5.6mm Assy FDA UDI
Model / Reference
M056-SS-130 FDA UDI
Description
Male Long Component for Ø5.6mm Assy FDA UDI

Identifiers

Catalog Number
M056-SS-130 FDA UDI
Primary DI / UDI-DI
07540194000156 FDA UDI
510(k) Number
K020885 FDA UDI
K041393 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5.6 Millimeter FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

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

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6b59173d-0d93-41e5-8d56-565355901435 38 fields · synced Jun 8, 2026