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MiiS 1802

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 Number04719872711230 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  • Withdrawn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
Generic Name
Ophthalmic tonometer, professional
Model / Reference
1802
Primary DI / UDI-DI
04719872711230
FDA Product Code
HKX
GMDN Term
Ophthalmic tonometer, professional
Device Class
Class II
Regulation Number
886.1930
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
  • Manufacturing Date

Other properties (11)

  • 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