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Vivatmo pro F09G100510

by Bosch Healthcare Solutions GmbH

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04059233001274 UDI-DI Date8 Jul 2024ListedStatusListed GUDID: 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  • Withdrawn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
Vivatmo pro
Generic Name
Electrochemical breath analyser IVD, point-of-care
Model / Ref / Catalog
F09G100510
Primary DI / UDI-DI
04059233001274
FDA Product Code
MXA
GMDN Term
Electrochemical breath analyser IVD, point-of-care
Device Class
Class II
Regulation Number
862.3080
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrochemical breath analyser IVD, point-of-care

Other devices from Bosch Healthcare Solutions GmbH

See all devices from Bosch Healthcare Solutions GmbH →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

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