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Dekenblok

EUDAMED

Class I (EU MDR)

Ref 7774

by Rebacare B.v.

Identity

Trade Name
Dekenblok EUDAMED
Device Name
Dekenblok EUDAMED
Model / Reference
7774 EUDAMED

Identifiers

Primary DI / UDI-DI
08720256429036 EUDAMED
Basic UDI-DI
87202564297774V5 EUDAMED
Direct Marketing DI
08720256429036 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Dekenblok by Rebacare B.v. — 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
Rebacare B.v.
EUDAMED SRN
NL-MF-000006751

Sources (1)

  • EUDAMED 58875564-d529-40f2-aaee-771e1ab8d604 61 fields · synced Jun 18, 2026