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Dmi 619-5140-1900

by Dms Holdings, Inc., 2 variants

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 Number00041298995043 UDI-DI Date30 Dec 2025ListedStatusListed 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  • Withdrawn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
Dmi
Generic Name
Electric pad localized-body heating system
Model / Reference
619-5140-1900
Primary DI / UDI-DI
00041298995043
FDA Product Code
IRT
GMDN Term
Electric pad localized-body heating system
Device Class
Class II
Regulation Number
890.5740
GUDID distribution status
In Commercial Distribution

Other devices from Dms Holdings, Inc.,

See all devices from Dms Holdings, Inc., →

Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

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