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Acteon Dock U USB Fedesa 7M Bien Air

by Sopro 2 variants

Acteon Dock U USB Fedesa 7M Bien Air (S_717_1507) is a Class II device made by Sopro, listed in FDA GUDID since 19 Nov 2018 (UDI-DI 03760278262094), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03760278262094 UDI-DI Date19 Nov 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Acteon
Generic name
Diagnostic-imaging multiformat camera
Model / Ref / Catalog
DOCK U USB FEDESA 7M BIEN AIR, S_717_1507
Primary DI / UDI-DI
03760278262094
FDA product code
NYH
GMDN term
Diagnostic-imaging multiformat camera
Device class
Class II
Regulation number
872.1740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Diagnostic-imaging multiformat camera

Similar devices in this category

Other devices filed under Diagnostic-imaging multiformat camera.

Other devices from Sopro

  • SOPIX2

    Class IIa

  • Sopix 2

    Class II

  • Sopix

    Class IIa

  • PSPIX2

    Class I

See all devices from Sopro →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)