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Agility Plus

by A.T.S. Applicazione Tecnologie Speciali s.r.l. 2 variants

Ref 74 09 000-3; 74 11 000-3Model ARCO FP

Active European Union EUDAMED: not on the EU market

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805518667FPVP Basic UDI-DIDate27 Apr 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  • Withdrawn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
ARCO FP, 74 09 000-3, 74 11 000-3
Primary DI / UDI-DI
08055186670884
Basic UDI-DI
805518667FPVP
Direct Marketing DI
08055186670884
EMDN Code
Z11039017 Mobile radioscopic units
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IT-MF-000010734

Other devices from A.T.S. Applicazione Tecnologie Speciali s.r.l.

See all devices from A.T.S. Applicazione Tecnologie Speciali s.r.l. →

Properties

Other properties (13)

  • Sterile: No
  • 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