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TTM011 Rozsdamentes infúziós pumpa dokkoló tartó állvány

by TakTiMed Egészségügyi, Kereskedelmi és Szolgáltató Kft.

Ref TTM011

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

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5999862367AllvanyokTM Basic UDI-DI 05999862367008UDI-DIDate13 Jul 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
TTM Rozsdamentes infúziós pumpa dokkoló tartó állványok
Model / Reference
TTM011
Primary DI / UDI-DI
05999862367008
Basic UDI-DI
5999862367AllvanyokTM
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000029587

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from TakTiMed Egészségügyi, Kereskedelmi és Szolgáltató Kft.

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