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Acteon Soprocare N

by Sopro

Acteon Soprocare N (997092) is a Class II device made by Sopro, listed in FDA GUDID since 12 Mar 2019 (UDI-DI 03760278260199), 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 Number03760278260199 UDI-DI Date12 Mar 2019ListedStatusListed 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  • Withdrawn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
SOPROCARE N, 997092
Primary DI / UDI-DI
03760278260199
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

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)