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cvi42 5.6

by Circle Cardiovascular Imaging

cvi42 5.6 is a Class II device made by Circle Cardiovascular Imaging, listed in FDA GUDID since 28 Jul 2017 (UDI-DI 00882916000004), 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 Number00882916000004 UDI-DI Date28 Jul 2017ListedStatusListed 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  • Withdrawn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
cvi42
Generic name
MRI system application software
Model / reference
5.6
Primary DI / UDI-DI
00882916000004
FDA product code
LLZ
GMDN term
MRI system application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: MRI system application software

Similar devices in this category

Other devices filed under MRI system application software.

Other devices from Circle Cardiovascular Imaging

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Properties

  • Prescription use
Other properties (14, all answered No)