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Cleartrace 1700-001

by Conmed Corporation

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

1 closed

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 Number10653405004226 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Recalls

1 recall · FDA

    • Terminated Z-1185-03 FDA Unclassified (pre-2012) initiated 30 Jul 2003

    Separation of the sensing element from the body of the electrode.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Cleartrace
Generic Name
Electrocardiographic electrode, single-use
Model / Ref / Catalog
1700-001
Primary DI / UDI-DI
10653405004226
510(k) Number
FDA Product Code
DRX
GMDN Term
Electrocardiographic electrode, single-use
Device Class
Class II
Regulation Number
870.2360
GUDID distribution status
Not in Commercial Distribution

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: 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
  • Manufacturing Date: No