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Tasectan 15 capsules

by Noventure S.L.U.

Ref 1308500Model Tasectan capsules

Active European Union

CE MDR

Valid until

21 Dec 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier ISTITUTO SUPERIORE DI SANITA'

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0016230226 Date26 Feb 2026IssuedStatusActive expires 21 Dec 2028

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • CSQ0016230226 Active Amended

    Quality management system EU MDR

    Issued
    26 Feb 2026
    Expires
    21 Dec 2028
    Reason
    Mnf data change
  • CVD0023230226 Active Amended

    Technical documentation EU MDR

    Issued
    26 Feb 2026
    Expires
    21 Dec 2028
    Reason
    Mnf data change

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Tasectan capsules
Model / Reference
Tasectan capsules, 1308500
Primary DI / UDI-DI
08436593830151
Basic UDI-DI
843659383TAS123LX
Direct Marketing DI
08436593830151
EMDN Code
G99 Gastrointestinal devices - other
Device Class
Class III
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
ES-MF-000000797

Other devices from Noventure S.L.U.

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Properties

  • Animal Tissues

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No