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Vivatmo pro Level 0 F09G100230

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 Number04059233000307 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  • Withdrawn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 Level 0
Generic Name
Electrochemical breath analyser filter/mouthpiece IVD
Model / Ref / Catalog
F09G100230
Primary DI / UDI-DI
04059233000307
FDA Product Code
MXA
GMDN Term
Electrochemical breath analyser filter/mouthpiece IVD
Device Class
Class II
Regulation Number
862.3080
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrochemical breath analyser filter/mouthpiece IVD

Other devices from Bosch Healthcare Solutions GmbH

See all devices from Bosch Healthcare Solutions GmbH →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No