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Maxostom™ Ostomy Baseplate

by Meril Medical Innovations Private Limited 15 variants

Ref MOB70FSModel Model 1,2,3,4,5,6,7,8,9,10,11,12,13,14 and15

Withdrawn Withdrawn in European Union.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

Was authorized under CE MDR, withdrawn

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Withdrawn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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8909121OBPJN Basic UDI-DI 08909121018265UDI-DIDate10 Oct 2026RegisteredStatusWithdrawn 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

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
Ostomy Baseplate
Model / Reference
Model 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 and15, MOB70FS
Primary DI / UDI-DI
08909121018265
Basic UDI-DI
8909121OBPJN
EMDN Code
A1002010101 Colostomy plates, with non-retracted stoma
Device Class
Class I

Manufacturer details

EUDAMED SRN
IN-MF-000045025
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

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