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MiiS Horus scope 5042

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 Number04719872710226 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  • Withdrawn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 scope
Generic Name
Rigid optical arthroscope, single-use
Model / Reference
5042
Primary DI / UDI-DI
04719872710226
FDA Product Code
HRX
GMDN Term
Rigid optical arthroscope, single-use
Device Class
Class II
Regulation Number
888.1100
GUDID distribution status
In Commercial Distribution

Other devices from Medimaging Integrated Solution, Inc (Miis)

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

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No