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CATCHView Thrombo-embolectomy device

by Balt extrusion SAS 8 variants

Ref CATCHVMINI20

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-03700481331262 Basic UDI-DI 03700481331262UDI-DIDate5 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

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 32 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 1 Jan 2018
  • Belgium since 1 Jan 2018
  • Bulgaria since 1 Jan 2018
  • Croatia since 1 Jan 2018
  • Cyprus since 1 Jan 2018
  • Czechia since 1 Jan 2018
  • Denmark since 1 Jan 2018
  • Estonia since 1 Jan 2018
  • Finland since 1 Jan 2018
  • France since 1 Jan 2018
  • Germany since 1 Jan 2018
  • Greece since 1 Jan 2018
  • Hungary since 1 Jan 2018
  • Iceland since 1 Jan 2018
  • Ireland since 1 Jan 2018
  • Italy since 1 Jan 2018
  • Latvia since 1 Jan 2018
  • Liechtenstein since 1 Jan 2018
  • Lithuania since 1 Jan 2018
  • Luxembourg since 1 Jan 2018
  • Malta since 1 Jan 2018
  • Netherlands since 1 Jan 2018
  • Northern Ireland since 1 Jan 2018
  • Norway since 1 Jan 2018
  • Poland since 1 Jan 2018
  • Portugal since 1 Jan 2018
  • Romania since 1 Jan 2018
  • Slovakia since 1 Jan 2018
  • Slovenia since 1 Jan 2018
  • Spain since 1 Jan 2018
  • Sweden since 1 Jan 2018
  • Türkiye since 1 Jan 2018

Last checked 27 Oct 2026.

Specification

EUDAMED

Device Name
CATCHView Thrombo-embolectomy device
Model / Reference
CATCHVMINI20
Primary DI / UDI-DI
03700481331262
Basic UDI-DI
B-03700481331262
EMDN Code
C010402020701 Manual peripheral thrombectomy and thromboaspiration systems
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000007563

Other devices from Balt extrusion SAS

See all devices from Balt extrusion SAS →

Properties

  • Sterile

Other properties (12)

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