Contagocce 18 N + tige vetro matita h59 + pomp. Verde + copritge

by Remy & Geiser GmbH

Ref 12241

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number805513664PIPETTETA Basic UDI-DI 08055136643463UDI-DI	Date16 Sep 2024Registered	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Withdrawn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: Contagocce 18 N + tige vetro matita h59 + pomp. Verde + copritge
Model / Reference: 12241

Primary DI / UDI-DI: 08055136643463
Basic UDI-DI: 805513664PIPETTETA
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000020726

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Properties

Administering Medicine

Other properties (12)

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
Measuring Function: No
Incorporates Medicinal Product: No