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MR Patient Care Wide ECG 3.0 Cable AAMI Expression MR ECG Leads, AAMI, CV

by Philips Ds North America LLC

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 Number00884838054899 UDI-DI Date30 Sep 2016ListedStatusListed 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  • Withdrawn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
MR Patient Care Wide ECG 3.0 Cable AAMI
Generic Name
Electrocardiographic lead set, reusable
Model / Ref / Catalog
Expression MR ECG Leads, AAMI, CV, 989803193721
Primary DI / UDI-DI
00884838054899
FDA Product Code
MWI
GMDN Term
Electrocardiographic lead set, reusable
Device Class
Class II
Regulation Number
870.2300
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

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Properties

  • Prescription Use
  • Serial Number

Other properties (12)

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