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Single Use Rotatable and Repositionable Hemoclip

EUDAMED

Class IIb (EU MDR)

Ref HA-Ⅲ-5C

by Anrei Medical (HZ) Co., Ltd.

Identity

Device Name
Single Use Rotatable and Repositionable Hemoclip EUDAMED
Model / Reference
HA-Ⅲ-5C EUDAMED

Identifiers

Primary DI / UDI-DI
06926839810907 EUDAMED
Basic UDI-DI
694831892b004MJ EUDAMED
EMDN Code
G030202 DIGESTIVE ENDOSCOPY, HAEMOSTASIS CLIPS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

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

Single Use Rotatable and Repositionable Hemoclip by Anrei Medical (HZ) CO., LTD. — Class IIb — 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-000009964
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED fb78a94b-297f-48dd-9e5a-8aed079ffce5 61 fields · synced Jun 18, 2026