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Arterys Cardio DL CVM2

by Arterys Inc. 2 variants

Arterys Cardio DL CVM2, a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Arterys Inc., was listed in FDA GUDID on 23 Jun 2018 (UDI-DI B664CVM20); the registry lists it as 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 NumberB664CVM20 UDI-DI Date23 Jun 2018ListedStatusListed 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  • Withdrawn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
Arterys Cardio DL
Generic name
Radiology DICOM image processing application software
Model / reference
CVM2
Primary DI / UDI-DI
B664CVM20
FDA product code
LLZ
GMDN term
Radiology DICOM image processing application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).

Other devices from Arterys Inc.

See all devices from Arterys Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)