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CELERUS Kek Detektalhato

EUDAMED

Class I (EU MDR)

Ref Kek Detektalhato

by Suzhou Sunmed Co., Ltd.

Identity

Trade Name
CELERUS Kek Detektalhato EUDAMED
Device Name
CELERUS AluDerm adhesive bandage EUDAMED
Model / Reference
Kek Detektalhato EUDAMED

Identifiers

Primary DI / UDI-DI
06973864851269 EUDAMED
Basic UDI-DI
697386485CELERUS7D EUDAMED
EMDN Code
M04010199 ADHESIVE DRESSINGS, WITH ABSORBENT PAD - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Hungary 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

CELERUS Kek Detektalhato by Suzhou Sunmed Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000010170
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 3f03a17c-aaff-420c-8c38-928ec3c73730 61 fields · synced Jun 19, 2026