eudamed_udi
Primary ID: 08436557230805
Neumobit (UDI 08436557230805)
Manufactured by Medical Respiratory Devices S.L
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neumobit - Primary ID 08436557230805
Device Regulatory Overview
The Neumobit (Model/Catalog Number: MRMB-01) is a medical device manufactured by Medical Respiratory Devices S.L. This product is indexed under FDA Product Code / Category Classification Z12150185 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MRMB-01
- Product Code / EMDN
- Z12150185
- Device Name
- Neumobit
- Database Sync Date
- 2026-08-09 18:04:14
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 Neumobit?
The registered manufacturer of record for Neumobit is Medical Respiratory Devices S.L.
What is the Primary UDI-DI identifier for Neumobit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436557230805.
What classification code is assigned to this device?
This device is registered under product classification code Z12150185.
Similar Classification Devices (Z12150185)
Other Devices by Medical Respiratory Devices S.L
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