Single Use Rotatable and Repositionable Hemoclip

by Anrei Medical (Hangzhou) Co., Ltd. 127 variants

Ref CMHC829132

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number694831892b004MJ Basic UDI-DI 06948318917129UDI-DI	Date25 Feb 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Single Use Rotatable and Repositionable Hemoclip
Model / Reference: CMHC829132

Primary DI / UDI-DI: 06948318917129
Basic UDI-DI: 694831892b004MJ
EMDN Code: G030202 Digestive endoscopy, haemostasis clips

Device Class: Class IIb
EU market of registration: Austria

Manufacturer details

EUDAMED SRN: CN-MF-000009964
Authorised representative: Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Anrei Medical (Hangzhou) Co., Ltd.

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Single Use Rotatable and Repositionable Hemoclip

Class IIb
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Single-use Balloon Dilator Catheter

Class IIa
Sphincterotome

Class IIb
Polypectomy Snare

Class IIb

See all devices from Anrei Medical (Hangzhou) Co., Ltd. →

Properties

Sterile
Implantable
Sutures

Other properties (11)

Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No