Sponge Stick

by GRI Medical & Electronic Technology Co., Ltd. 12 variants

Ref 25-2009C-S2

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number69319181F011KN Basic UDI-DI 16931918110578UDI-DI	Date16 Oct 2022Registered	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Withdrawn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: Sponge Stick
Model / Reference: 25-2009C-S2

Primary DI / UDI-DI: 16931918110578
Basic UDI-DI: 69319181F011KN
Unit of Use DI: 06931918110571
EMDN Code: V9012 Non-specialist surgical instruments and kits, single-use

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

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