Hydrophilic Intermittent Catheter

by Hangzhou Bever Medical Devices Co., Ltd. 12 variants

Ref 386M10

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number69487962NC0002Q6 Basic UDI-DI 16948796231660UDI-DI	Date27 Jun 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Withdrawn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

Model / Reference: 386M10

Primary DI / UDI-DI: 16948796231660
Basic UDI-DI: 69487962NC0002Q6
EMDN Code: U01010502 Nelaton catheters, non self-lubricating

Device Class: Class I
EU market of registration: Greece

Manufacturer details

EUDAMED SRN: CN-MF-000018408
Authorised representative: Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Hangzhou Bever Medical Devices Co., Ltd.

Nasopharygeal Airway

Class I
Hydrophilic Intermittent Catheter

Class I
Pre-Lubricated Hydrophilic Catheter

Class I
Nasopharyngeal Airway

Class I
Nasopharygeal Airway

Class I
Nasopharygeal Airway

Class I

See all devices from Hangzhou Bever Medical Devices Co., Ltd. →

Properties

Sterile

Other properties (12)

Implantable: No
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