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JETi™ WVCART

by Abbott Vascular

JETi™ WVCART is a Class I device made by Abbott Vascular, listed in FDA GUDID since 8 Dec 2021 (UDI-DI 08717648351372), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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 Number08717648351372 UDI-DI Date8 Dec 2021ListedStatusListed GUDID: 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  • Withdrawn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
JETi™
Generic name
Medical device integration rack
Model / Ref / Catalog
WVCART
Primary DI / UDI-DI
08717648351372
FDA product code
FOX
GMDN term
Medical device integration rack
Device class
Class I
Regulation number
880.6990
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical device integration rack

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Other devices filed under Medical device integration rack.

Other devices from Abbott Vascular

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Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)