Skip to content

Intraveno™

by Mais India Medical Devices Pvt. Ltd. 3 variants

Ref MI/CA/01-000-EModel Foley Balloon Catheter - Latex/Silicon (2 Way/3 Way), I.V. Cannula/Catheter with injection port and with wings 14G

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number890606548U03NS Basic UDI-DI Date12 Mar 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  • Withdrawn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

Device Name
Foley Balloon Catheter
I.V. Cannula/Catheter
Model / Reference
Foley Balloon Catheter - Latex/Silicon (2 Way/3 Way), MI/CA/01-000-E, I.V. Cannula/Catheter with injection port and with wings 14G
Primary DI / UDI-DI
08904476805430, 08906065482756, 08904476805195, 08904476805294, 08904476805416, 08906065482770, 08904476805492, 08904476805454, 08906065486587, 08904476805485, 08904476805249, 08906065486853, 08904476805409, 08904476805508, 08906065486617, 08904476805119, 08906065486914, 08904476805355, 08904476805386, 08904476805188, 08904476805201, 08906065482794, 08904476805447, 08904476805171, 08904476805133, 08904476805324, 08904476805348, 08906065486884, 08904476805461, 08904476805140, 08906065486624, 08904476805287, 08904476805096, 08904476805423, 08906065486600, 08904476805331, 08906065486594, 08906065486648, 08904476805522, 08906065482787, 08904476805393, 08904476805102, 08906065482763, 08904476805263
Basic UDI-DI
890606548U03NS, 890606548I01LS
Direct Marketing DI
08904476805430
08906065482756
08904476805195
08904476805294
08904476805416
08906065482770
08904476805492
08904476805454
08906065486587
08904476805485
08904476805249
08906065486853
08904476805409
08904476805508
08906065486617
08904476805119
08906065486914
08904476805355
08904476805386
08904476805188
08904476805201
08906065482794
08904476805447
08904476805171
08904476805133
08904476805324
08904476805348
08906065486884
08904476805461
08904476805140
08906065486624
08904476805287
08904476805096
08904476805423
08906065486600
08904476805331
08906065486594
08906065486648
08904476805522
08906065482787
08904476805393
08904476805102
08906065482763
08904476805263
EMDN Code
U0199, U020199, C0101010101, C0101010102
Device Class
Class IIa
EU market of registration
Greece
Ireland
Estonia
Hungary
Bulgaria
Czechia
Cyprus
Germany
Croatia
Iceland
Austria
Finland
Denmark
Belgium
Latvia
Luxembourg

Manufacturer details

EUDAMED SRN
IN-MF-000021842
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Mais India Medical Devices Pvt. Ltd.

See all devices from Mais India Medical Devices Pvt. Ltd. →

Properties

  • Sterile
  • Contains Latex NoEUDAMEDYesEUDAMED
  • Administering Medicine NoEUDAMEDYesEUDAMED

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No