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Steinfänger, wiederverwendbar

by MTW - Endoskopie W. Haag KG 13 variants

Ref 110101210

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 linked in EUDAMED

A group certificate may exist

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 Number4046223G0305010202AREABQB Basic UDI-DI 04046223009013UDI-DIDate13 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
Sprühkatheter, wiederverwendbar
Device Name
Steinfänger, wiederverwendbar
Sonden
Model / Reference
110101210
Primary DI / UDI-DI
04046223009013
Basic UDI-DI
4046223G0305010202AREABQB, 4046223G020199XXXXBRXXXX7
EMDN Code
G020199 Gastrointestinal lavage, tubes and sets - other
Device Class
Class IIa
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000004993

Other devices from MTW - Endoskopie W. Haag KG

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Properties

  • Sterile

Other properties (12)

  • 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