gudid
Primary ID: F09G100230
Vivatmo pro Level 0 (UDI F09G100230)
Manufactured by Bosch Healthcare Solutions GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vivatmo pro Level 0 - Primary ID F09G100230
Device Regulatory Overview
The Vivatmo pro Level 0 (Model/Catalog Number: F09G100230) is a medical device manufactured by Bosch Healthcare Solutions GmbH. This product is indexed under FDA Product Code / Category Classification MXA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F09G100230
- Product Code / EMDN
- MXA
- Device Name
- Disposable mouthpiece for Vivatmo
- Database Sync Date
- 2026-08-09 09:11:48
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Vivatmo pro Level 0?
The registered manufacturer of record for Vivatmo pro Level 0 is Bosch Healthcare Solutions GmbH.
What is the Primary UDI-DI identifier for Vivatmo pro Level 0?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is F09G100230.
What classification code is assigned to this device?
This device is registered under product classification code MXA.
Similar Classification Devices (MXA)
Other Devices by Bosch Healthcare Solutions GmbH
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