BOSCH HEALTHCARE SOLUTIONS GMBH

FDA Device Registration & Listing · Waiblingen Baden-Wurttemberg, DE · Registration 3001082393

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3001082393
FEI Number
3001082393
Entity Name
BOSCH HEALTHCARE SOLUTIONS GMBH
City/State/Country
Waiblingen Baden-Wurttemberg, DE
Establishment Address
Alte Bundesstrasse 50, Waiblingen Baden-Wurttemberg 71332, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Bosch Healthcare Solutions GmbH (Owner Number: 10090281)
Owner / Operator Contact Address
Alte Bundesstrasse 50, Waiblingen, DE-BW 71332, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Vivatmo pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MXA System, Test, Breath Nitric Oxide Clinical Toxicology Class 2 862.3080 2024-03-07

Official Correspondent

Jeannette Stroh

US Agent Details

David Petrich Business: Landrich Group Email: david@landrichgroup.com Phone: (925) 5968902

Related Public Records

Same Entity

Bosch Healthcare Solutions GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001082393. Last updated year: 2026. Please use registration number 3001082393 when referencing this establishment in official correspondence.
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