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Mui Scientific S7-R24-1047

by H & A Mui Enterprises Inc

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number10678467508451 UDI-DI Date11 Aug 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Mui Scientific
Generic Name
Gastrointestinal motility manometric catheter, non-electronic
Model / Reference
S7-R24-1047
Primary DI / UDI-DI
10678467508451
510(k) Number
FDA Product Code
FFX
GMDN Term
Gastrointestinal motility manometric catheter, non-electronic
Device Class
Class II
Regulation Number
876.1725
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K823701)

Show all (12)

Other devices from H & A Mui Enterprises Inc

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Properties

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

Other properties (10)

  • Sterile: No
  • 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