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IST Set 22+ AP 209 Sapphire

by IST Medical GmbH

Ref 101049Model IST Set 22+ AP 209 Sapphire

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++EIST101049KJ Basic UDI-DI +EIST1010490GUDI-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  • Withdrawn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 22+ AP 209 Sapphire, 101049
Primary DI / UDI-DI
+EIST1010490G
Basic UDI-DI
++EIST101049KJ
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

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Properties

  • Sterile