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Stomafit Stoma Stopper FR08 LG60 ST08-60

by Hoist Medical

Ref ST08-60Model STOMAFIT STOMA STOPPER ST08-30

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 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376034811100.05B3 Basic UDI-DI 03760348112250UDI-DIDate9 Oct 2025RegisteredStatusActive

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  • Withdrawn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
Stomafit Stoma Stopper ST08-30
Model / Reference
STOMAFIT STOMA STOPPER ST08-30, ST08-60
Primary DI / UDI-DI
03760348112250
Basic UDI-DI
376034811100.05B3
Direct Marketing DI
03760348112250
EMDN Code
G0280 Gastrointestinal tubes - accessories
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000026140

Other devices from Hoist Medical

See all devices from Hoist Medical →

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