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Bentonit MED Detox Pulver

by Natur Vital Handels GmbH 57 variants

Ref B200NLModel Bentonite powder BP

Active European Union

CE MDR

Valid until

2 Nov 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Eurofins Product Testing Italy S.r.l.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberEPT 0477.MDR.23/5278.1 Date31 Oct 2025IssuedStatusActive expires 2 Nov 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.23/5278.1 Active Reissued

    Quality management system EU MDR

    Certifier
    Eurofins Product Testing Italy S.r.l. 0477
    Issued
    31 Oct 2025
    Expires
    2 Nov 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Bentonite powder BP, B200NL
Primary DI / UDI-DI
09120127213082
Basic UDI-DI
912012721BPN6
EMDN Code
G0402 Orally administered devices for appetite control and reduction of intestinal absorption
Device Class
Class IIb
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
AT-MF-000026484

Other devices from Natur Vital Handels GmbH

See all devices from Natur Vital Handels GmbH →

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