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Alco-Swab

EUDAMED

Class I (EU MDR)

Ref HOS-10-4300HD

by Hospidex France SAS

Identity

Trade Name
Alco-Swab EUDAMED
Device Name
Alco-Swab EUDAMED
Model / Reference
HOS-10-4300HD EUDAMED

Identifiers

Primary DI / UDI-DI
05425018680535 EUDAMED
Basic UDI-DI
542501868ALCOSWAB000000AC 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-Swab 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 2950cf01-89f5-436e-b87f-14786613ead3 61 fields · synced Jun 18, 2026