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VeinViewer 3.0 Flex

by Christie Medical Holdings, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 17 Oct 2026. What this means

Regulatory status

as of registry sync 17 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM870134002102021 UDI-DI Date14 Sep 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Hand-held multi-spectral vascular imaging device
Model / Ref / Catalog
3.0 Flex, 134-002102-02
Primary DI / UDI-DI
M870134002102021
FDA Product Code
KZA
GMDN Term
Hand-held multi-spectral vascular imaging device
Device Class
Class I
Regulation Number
880.6970
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hand-held multi-spectral vascular imaging device

Other devices from Christie Medical Holdings, Inc.

Properties

  • Prescription Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No