Securement Device

by GRI Medical & Electronic Technology Co., Ltd. 5 variants

Ref 10-519027

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number69319181F005KT Basic UDI-DI 16931918131016UDI-DI	Date22 Jun 2023Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Securement Device
Model / Reference: 10-519027

Primary DI / UDI-DI: 16931918131016
Basic UDI-DI: 69319181F005KT
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: CN-MF-000004203
Authorised representative: Emergo Europe B.V. NL-AR-000000116

Other devices from GRI Medical & Electronic Technology Co., Ltd.

Underpads

Class I
Surgical Drapes

Class I
Equipment Covers

Class I
Procedure pack

Class IIa
Surgical Gowns

Class I
Basins and Trays

Class I

See all devices from GRI Medical & Electronic Technology Co., Ltd. →

Properties

Other properties (13)

Sterile: No
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