plastic pill cutter

by Guangzhou Athmedic Healthcare Co., Ltd

Ref AM10-004

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR

Ended

Withdrawn

Date not published (CE MDR)

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697620128ppillcuttera7K Basic UDI-DI 06976201280364UDI-DI	Date4 Jun 2025Registered	StatusWithdrawn No longer placed on the EU market

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Withdrawn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European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name: plastic pill cutter
Model / Reference: AM10-004

Primary DI / UDI-DI: 06976201280364
Basic UDI-DI: 697620128ppillcuttera7K
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I

Manufacturer details

EUDAMED SRN: CN-MF-000011674
Authorised representative: SUNGO Europe B.V. NL-AR-000000247

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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