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IST Set 20 Ambix activ

by IST Medical GmbH

Ref 200861Model IST Set 20 Ambix activ

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 Number++EIST200861LN Basic UDI-DI +EIST2008610IUDI-DIDate21 Oct 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  • Withdrawn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

Model / Reference
IST Set 20 Ambix activ, 200861
Primary DI / UDI-DI
+EIST2008610I
Basic UDI-DI
++EIST200861LN
EMDN Code
A03040199 Infusion kits (with or w/o pump), single-use - other
Device Class
Class I
Medical Purpose
Set für die parenterale Versorgung

Manufacturer details

EUDAMED SRN
DE-PR-000021824

Other devices from IST Medical GmbH

See all devices from IST Medical GmbH →

Properties

  • Sterile