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IST Set 8A+ Portnadelwechsel

by IST Medical GmbH

Ref 101019Model IST Set 8A+ Portnadelwechsel

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EIST101019K9 Basic UDI-DI +EIST1010190DUDI-DIDate15 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  • Withdrawn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 8A+ Portnadelwechsel, 101019
Primary DI / UDI-DI
+EIST1010190D
Basic UDI-DI
++EIST101019K9
EMDN Code
A01010301 Needles and kits for implantable systems (port), with safety systems
Device Class
Class I
Medical Purpose
Set für den sterilen Portnadelwechsel

Manufacturer details

EUDAMED SRN
DE-PR-000021824

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Properties

  • Sterile