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CorPath Interventional Cockpit 101

by Corindus, Inc.

CorPath Interventional Cockpit 101 is a Class I device made by Corindus, Inc., listed in FDA GUDID since 16 Nov 2016 (UDI-DI 00816280021013), 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 Number00816280021013 UDI-DI Date16 Nov 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  • Withdrawn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 Interventional Cockpit
Generic name
Radiation shielding panel, portable/mobile
Model / Ref / Catalog
101
Primary DI / UDI-DI
00816280021013
FDA product code
IWX
GMDN term
Radiation shielding panel, portable/mobile
Device class
Class I
Regulation number
892.6500
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Radiation shielding panel, portable/mobile

Similar devices

Other devices filed under FDA product code IWX (Barrier, Control Panel, X-Ray, Movable).

Other devices from Corindus, Inc.

See all devices from Corindus, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)