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Gap Endo-Exo Medullary System

FDA UDI

Class II (US FDA UDI)

by Orthopediatrics Canada ULC

Identity

Trade Name
GAP ENDO-EXO MEDULLARY SYSTEM FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
NAIL 2.0 Ø4.8mm x 260mm FDA UDI
Model / Reference
GAP-2N48-26 FDA UDI
Description
NAIL 2.0 Ø4.8mm x 260mm FDA UDI

Identifiers

Catalog Number
GAP-2N48-26 FDA UDI
Primary DI / UDI-DI
07540194016201 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
Length — 260 Millimeter FDA UDI
Outer Diameter — 4.8 Millimeter FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

Gap Endo-Exo Medullary 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4136e464-24c3-4ca4-abd8-362bb7d972c5 36 fields · synced May 31, 2026