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Mabis 10-422-010

by Dms Holdings, Inc.,

Listed FDA GUDID listing, not in commercial distribution

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 Number00767056422018 UDI-DI Date29 Dec 2025ListedStatusListed GUDID: not 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  • Withdrawn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
Mabis
Generic Name
Mechanical external stethoscope
Model / Reference
10-422-010
Primary DI / UDI-DI
00767056422018
FDA Product Code
LDE
GMDN Term
Mechanical external stethoscope
Device Class
Class I
Regulation Number
870.1875
GUDID distribution status
Not 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