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CorPath 200 Control Console 160-00043

by Corindus, Inc.

CorPath 200 Control Console 160-00043 is a Class II device made by Corindus, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00816280022010), not in commercial distribution (GUDID) as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816280022010 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
CorPath 200 Control Console
Generic name
Cardiac mapping system workstation
Model / Ref / Catalog
160-00043
Primary DI / UDI-DI
00816280022010
FDA product code
DXX
GMDN term
Cardiac mapping system workstation
Device class
Class II
Regulation number
870.1290
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code DXX (System, Catheter Control, Steerable).

Other devices from Corindus, Inc.

See all devices from Corindus, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)