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FARGO guiding catheter

by Balt extrusion SAS 36 variants

Ref FRGMAX6F115_8MP

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-03700481333730 Basic UDI-DI 03700481333730UDI-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  • Withdrawn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 19 Feb 2009
  • Belgium since 19 Feb 2009
  • Bulgaria since 19 Feb 2009
  • Croatia since 19 Feb 2009
  • Cyprus since 19 Feb 2009
  • Czechia since 19 Feb 2009
  • Denmark since 19 Feb 2009
  • Estonia since 19 Feb 2009
  • Finland since 19 Feb 2009
  • France since 19 Feb 2009
  • Germany since 19 Feb 2009
  • Greece since 19 Feb 2009
  • Hungary since 19 Feb 2009
  • Iceland since 19 Feb 2009
  • Ireland since 19 Feb 2009
  • Italy since 19 Feb 2009
  • Latvia since 19 Feb 2009
  • Liechtenstein since 19 Feb 2009
  • Lithuania since 19 Feb 2009
  • Luxembourg since 19 Feb 2009
  • Malta since 19 Feb 2009
  • Netherlands since 19 Feb 2009
  • Northern Ireland since 19 Feb 2009
  • Norway since 19 Feb 2009
  • Poland since 19 Feb 2009
  • Portugal since 19 Feb 2009
  • Romania since 19 Feb 2009
  • Slovakia since 19 Feb 2009
  • Slovenia since 19 Feb 2009
  • Spain since 19 Feb 2009
  • Sweden since 19 Feb 2009
  • Türkiye since 19 Feb 2009

Last checked 24 Oct 2026.

Specification

EUDAMED

Device Name
FARGO guiding catheter
Model / Reference
FRGMAX6F115_8MP
Primary DI / UDI-DI
03700481333730
Basic UDI-DI
B-03700481333730
EMDN Code
C0104020204 Peripheral angiography guide catheters
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000007563

From the manufacturer

Manufacturer's product page: Fargo Guiding Catheter

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