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AspireCath

by İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş. 2 variants

Ref CA0056, CA0057, CA0055, CA0058

Active European Union

CE MDD

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/MDD NumberB-868141006056749 Basic UDI-DI Date25 Jan 2024RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
AspireCath Catheter III, ID:0,7 mm 90 cm
AspireCath Catheter IV, ID:0,7 mm 100 cm
AspireCath Catheter II, ID:0,5 mm 100 cm
AspireCath Catheter V, ID:0,7 mm 110 cm
Model / Reference
CA0056, CA0057, CA0055, CA0058
Primary DI / UDI-DI
D-868141006056749, D-868141006057446, D-86814100605503Q, D-868141006058143
Basic UDI-DI
B-868141006056749, B-868141006057446, B-86814100605503Q, B-868141006058143
EMDN Code
C0104020202 Peripheral embolisation catheters and microcatheters
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019963

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Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No