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Alco-Prep

EUDAMED

Class I (EU MDR)

Ref HOS-610HD

by Hospidex France SAS

Identity

Trade Name
Alco-Prep EUDAMED
Device Name
Alco-Prep Large EUDAMED
Model / Reference
HOS-610HD EUDAMED

Identifiers

Primary DI / UDI-DI
05425018680511 EUDAMED
Basic UDI-DI
542501868ALCOPREPLARGE0AX EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Category: Device sterilization/disinfection container, reusable

Alco-Prep by Hospidex France SAS — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Hospidex France SAS
EUDAMED SRN
FR-MF-000008923

Sources (1)

  • EUDAMED 933ecdef-b395-48e0-a13e-7893fb4c1925 61 fields · synced Jun 19, 2026