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Pull Thru™

by F R Galantai Manufacturing Company Limited 4 variants

Ref ZZ2242+1+SPUP+2200Model Single Patient Use Pack

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number942102849MDCCBPPFU Basic UDI-DI 09421028494540UDI-DIDate30 Mar 2023RegisteredStatusActive

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  • Withdrawn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

Model / Reference
Single Patient Use Pack, ZZ2242+1+SPUP+2200
Primary DI / UDI-DI
09421028494540
Basic UDI-DI
942102849MDCCBPPFU
EMDN Code
V070101 Endoscopes cleaning brushes - for generic use
Device Class
Class I
Medical Purpose
The contents of the procedure pack are single use brushes intended for the manual cleaning of endoscopes and other medical instruments which may have internal channels.

Manufacturer details

EUDAMED SRN
NZ-PR-000034534

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Properties

Other properties (1)

  • Sterile: No