MR Patient Care Short Wide ECG 2.0 Cable AAMI CAB, 4 LD, CV MRI ECG

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00884838006379 UDI-DI	Date29 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: MR Patient Care Short Wide ECG 2.0 Cable AAMI
Generic Name: Electrocardiographic lead set, reusable
Model / Ref / Catalog: CAB, 4 LD, CV MRI ECG, 9223

Primary DI / UDI-DI: 00884838006379
FDA Product Code: DSA
GMDN Term: Electrocardiographic lead set, reusable

Device Class: Class II
Regulation Number: 870.2900
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Conditional

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Properties

Prescription Use
Lot / Batch 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
Serial Number: No
Expiration Date: No
Manufacturing Date: No