Intrex

by Bonetech Medisys Pvt. Ltd. 62 variants

Ref BN104.T09.34Model Cannulated Humerus Nail

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number++G562INC5 Basic UDI-DI G562BN104T09340UDI-DI	Date20 Nov 2025Registered	StatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name: Intramedullary Nails
Model / Reference: Cannulated Humerus Nail, BN104.T09.34

Primary DI / UDI-DI: G562BN104T09340
Basic UDI-DI: ++G562INC5
EMDN Code: P09120201 Intramedullary nails

Device Class: Class IIb

Manufacturer details

EUDAMED SRN: IN-MF-000020462
Authorised representative: Amstermed B.V. NL-AR-000001971

Properties

Implantable
Sutures

Other properties (12)

Sterile: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No