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3M YMDLW5P

by Hygia Health Services, 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 Number10817357021018 UDI-DI Date30 Sep 2016ListedStatusListed 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  • Withdrawn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
3M
Generic Name
Electrocardiographic lead set, reprocessed
Model / Reference
YMDLW5P
Primary DI / UDI-DI
10817357021018
FDA Product Code
IKD
GMDN Term
Electrocardiographic lead set, reprocessed
Device Class
Class II
Regulation Number
890.1175
GUDID distribution status
Not in Commercial Distribution

Other devices from Hygia Health Services, Inc.

See all devices from Hygia Health Services, Inc. →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: 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