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Vdrive Drape 1

by Stereotaxis, Inc.

Vdrive Drape 1 (001-010056-1) is a Class II device made by Stereotaxis, Inc., listed in FDA GUDID since 1 Aug 2016 (UDI-DI M58800101005611), not in commercial distribution (GUDID) as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM58800101005611 UDI-DI Date1 Aug 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Vdrive Drape
Generic name
Cardiac mapping system workstation
Model / Ref / Catalog
1, 001-010056-1
Primary DI / UDI-DI
M58800101005611
FDA product code
DXX, DQX
GMDN term
Cardiac mapping system workstation
Device class
Class II
Regulation number
870.1290, 870.1330
GUDID distribution status
Not in Commercial Distribution

Similar devices

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

Other devices from Stereotaxis, Inc.

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  • Navigant

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See all devices from Stereotaxis, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)