Skip to content

ECG 9500-1762-01

by Zoll Medical Corporation

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number00847946021665 UDI-DI Date12 Sep 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ECG
Generic Name
Electrical-only medical device connection cable, reusable
Model / Reference
9500-1762-01
Primary DI / UDI-DI
00847946021665
FDA Product Code
MKJ, DRO, LDD, LIX, DQA
GMDN Term
Electrical-only medical device connection cable, reusable
Device Class
Class III
Regulation Number
870.5310, 870.5550, 870.5300, 870.5210, 870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rechargeable professional automated external defibrillator

Cleared under the same submission (K120907)

Show all (12)

Other devices from Zoll Medical Corporation

See all devices from Zoll Medical Corporation →

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