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Mucus Extractor

by Ningbo Greetmed Medical Instruments Co., Ltd. 2 variants

Ref GT017-200A

Active European Union

CE MDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06958627529302 Basic UDI-DI 06958627529302UDI-DIDate22 Jun 2026RegisteredStatusActive

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

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
GT017-200A
Primary DI / UDI-DI
06958627529302
Basic UDI-DI
B-06958627529302
EMDN Code
R0580 Respiratory system suction and dilatation systems - accessories not included in other classes
Device Class
Class IIa
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000009634
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Ningbo Greetmed Medical Instruments Co., Ltd.

See all devices from Ningbo Greetmed Medical Instruments Co., Ltd. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No