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Dmi 532-8035-0100

by Dms Holdings, 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 Number00041298803027 UDI-DI Date29 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  • Withdrawn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
Patient gown, reusable
Model / Reference
532-8035-0100
Primary DI / UDI-DI
00041298803027
FDA Product Code
OEA
GMDN Term
Patient gown, reusable
Device Class
Class I
Regulation Number
878.4040
GUDID distribution status
In Commercial Distribution

Other devices from Dms Holdings, Inc.,

See all devices from Dms Holdings, Inc., →

Properties

  • Premarket Exempt

Other properties (13)

  • 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
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No