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IST Set 21B+ AP 210 Sapphire An- & Abhängeset

by IST Medical GmbH

Ref 200926Model IST Set 21B+ AP 210 Sapphire An- & Abhängeset

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EIST200926LR Basic UDI-DI +EIST2009260KUDI-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  • Withdrawn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 21B+ AP 210 Sapphire An- & Abhängeset, 200926
Primary DI / UDI-DI
+EIST2009260K
Basic UDI-DI
++EIST200926LR
EMDN Code
A03040199 Infusion kits (with or w/o pump), single-use - other
Device Class
Class I
Medical Purpose
IST Set 21B+ AP 210 Sapphire An- & Abhängeset

Manufacturer details

EUDAMED SRN
DE-PR-000021824

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Properties

  • Sterile