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Gap Endo-Exo Medullary System

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref GAP-N64-22Model NAIL

by Orthopediatrics Canada ULC

Identity

Trade Name
The GAP Nail Endo-Exo Medullary System EUDAMED
GAP ENDO-EXO MEDULLARY SYSTEM FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
Nail Ø6.4mm X 220mm FDA UDI
Model / Reference
GAP-N64-22 EUDAMEDFDA UDI
NAIL EUDAMED
Description
Nail Ø6.4mm X 220mm FDA UDI

Identifiers

Catalog Number
GAP-N64-22 FDA UDI
Primary DI / UDI-DI
07540194000927 EUDAMEDFDA UDI
Basic UDI-DI
7540194GAP-NAILSZQ EUDAMED
FDA Product Code
HSB FDA UDI
EMDN Code
P09120201 INTRAMEDULLARY NAILS EUDAMED
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
888.3020 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

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

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

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 — 6.4 Millimeter FDA UDI
Length — 220 Millimeter FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

Gap Endo-Exo Medullary System by Orthopediatrics Canada ULC — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

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 52015564-0207-4692-a855-94111c570a6a 37 fields · synced Jun 19, 2026
  • EUDAMED 6fc363c5-35c1-4d12-8872-eaa36ea5ffb0 61 fields · synced Jun 19, 2026