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Acteon Dock MU_USB2 - Fedesa - 7M - S

by Sopro

Acteon Dock MU_USB2 - Fedesa - 7M - S (S_717_1036) is a Class II device made by Sopro, listed in FDA GUDID since 24 Sep 2016 (UDI-DI M430S71710361), 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 NumberM430S71710361 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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 MU_USB2 - FEDESA - 7M - S, S_717_1036
Primary DI / UDI-DI
M430S71710361
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.

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  • PSPIX2

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See all devices from Sopro →

Properties

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