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I0001407

by provita medical gmbh & co. kg

Part of a family of 281 devices: see the family page

Ref 173023

I0001407 (173023) is a Class I device made by provita medical gmbh & co. kg, registered in EUDAMED on 6 Jul 2026 (Basic UDI-DI 42601239304JA), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42601239304JA Basic UDI-DI 04260123937966UDI-DIDate6 Jul 2026RegisteredStatusActive

Official records

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  • Withdrawn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
IV-pole without base + accessories
Model / reference
173023
Primary DI / UDI-DI
04260123937966
Basic UDI-DI
42601239304JA
Direct marketing DI
04260123937966
EMDN code
Z12030380 Infusion instruments - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005332

Similar devices in this category

Other devices filed under INFUSION INSTRUMENTS - HARDWARE ACCESSORIES.

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Properties

Other properties (14, all answered No)