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MiiS Horus Video Box 5002

by Medimaging Integrated Solution Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04719872715023 UDI-DI Date29 Apr 2026ListedStatusListed 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  • Withdrawn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
MiiS Horus Video Box
Generic Name
Endoscopic video image processing unit
Model / Reference
5002
Primary DI / UDI-DI
04719872715023
FDA Product Code
EOB
GMDN Term
Endoscopic video image processing unit
Device Class
Class II
Regulation Number
874.4760
GUDID distribution status
In Commercial Distribution

Other devices from Medimaging Integrated Solution, Inc (Miis)

See all devices from Medimaging Integrated Solution, Inc (Miis) →

Properties

  • Prescription Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No