Corail Amt

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

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

No FDA recalls on record, checked 24 Oct 2026.

Trade Name

Corail Amt EUDAMED

Corail GUDID

Generic Name

Surgical instrument handle, non-torque-limiting

Device Name

Instrument Handle, Hip

Model / Ref / Catalog

9522-11-500, 952211500

Primary DI / UDI-DI

10603295230663

Basic UDI-DI

0603295a0047293

Direct Marketing DI

10603295230663

FDA Product Code

HTQ

EMDN Code

L091199 Orthopaedic prosthetics instruments, reusable - other

GMDN Term

Surgical instrument handle, non-torque-limiting

Device Class

Class I

Regulation Number

888.4540

Market of Registration

Ireland

GUDID distribution status

In Commercial Distribution

Sterilization Method

Moist Heat or Steam Sterilization

EUDAMED SRN

IE-MF-000007377

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