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ELLIK silicon tube

EUDAMED

Class I (EU MDR)

Ref P1010D

by Hangzhou Hawk Optical Electronic Instruments Co., Ltd.

Identity

Trade Name
ELLIK silicon tube EUDAMED
Device Name
ELLIK Evaluator EUDAMED
Model / Reference
P1010D EUDAMED

Identifiers

Primary DI / UDI-DI
06947014622733 EUDAMED
Basic UDI-DI
69470146RJ00176710U9 EUDAMED
EMDN Code
U090204 BLADDER EVACUATORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

ELLIK silicon tube by Hangzhou Hawk Optical Electronic Instruments 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-000028791
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED c8704a84-3b08-44a1-9c54-aed31907833e 61 fields · synced Jul 22, 2026