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ENDOGATOR Tubing

by Medivators Inc. 6 variants

Ref 4010682Model ENDOGATOR Tubing

ENDOGATOR Tubing (4010682) is a Class IIa device made by Medivators Inc., registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-00724995362928), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00724995362928 Basic UDI-DI 00724995362928UDI-DIDate6 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
ENDOGATOR Tubing, 4010682
Primary DI / UDI-DI
00724995362928
Basic UDI-DI
B-00724995362928
EMDN code
G020199 Gastrointestinal lavage, tubes and sets - other
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
US-MF-000043422
Authorised representative
STERIS Ireland Ltd IE-AR-000010065

Similar devices in this category

Other devices filed under GASTRO-INTESTINAL LAVAGE TUBES AND SETS.

Other devices from Medivators Inc.

See all devices from Medivators Inc. →

Properties

  • Supplied sterile
Other properties (13, all answered No)