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The GAP Nail Endo-Exo Medullary System

EUDAMEDFDA UDI

Class I (EU MDR)

Ref GAP-SGW116Model GUIDE WIRE SLEEVE

by OrthoPediatrics Canada ULC

Identity

Trade Name
The GAP Nail Endo-Exo Medullary System EUDAMED
GAP ENDO-EXO MEDULLARY SYSTEM FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
GAP GUIDE WIRE SLEEVE FOR 1.6mm GUIDE WIRE FDA UDI
Model / Reference
GUIDE WIRE SLEEVE EUDAMED
GAP-SGW116 EUDAMEDFDA UDI
Description
GAP GUIDE WIRE SLEEVE FOR 1.6mm GUIDE WIRE FDA UDI

Identifiers

Catalog Number
GAP-SGW116 FDA UDI
Primary DI / UDI-DI
07540194010193 EUDAMEDFDA UDI
Basic UDI-DI
7540194GAP-GWSQ6 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA 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

The GAP Nail Endo-Exo Medullary System by Orthopediatrics Canada Ulc — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CA-MF-000013010
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (2)

  • EUDAMED c3835684-cbbb-4446-b200-aa7067836d98 61 fields · synced Jun 19, 2026
  • FDA UDI 3d7b314e-6fad-403f-bba6-8dde3998d1b5 36 fields · synced May 30, 2026