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Veincas V800NV

by Shenzhen Vivolight Medical Device & Technology Co., Ltd.

Veincas V800NV is a Class I device made by Shenzhen Vivolight Medical Device & Technology Co., Ltd., listed in FDA GUDID since 20 Apr 2023 (UDI-DI 06971141530227), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06971141530227 UDI-DI Date20 Apr 2023ListedStatusListed 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  • Withdrawn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
Veincas
Generic name
Infrared-light vein locator
Model / reference
V800NV
Primary DI / UDI-DI
06971141530227
FDA product code
KZA
GMDN term
Infrared-light vein locator
Device class
Class I
Regulation number
880.6970
GUDID distribution status
In Commercial Distribution

Related devices

Category: Infrared-light vein locator

Other devices from Shenzhen Vivolight Medical Device & Technology Co., Ltd.

See all devices from Shenzhen Vivolight Medical Device & Technology Co., Ltd. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)