eudamed_udi
Primary ID: 08033480009074
INBRUSH (UDI 08033480009074)
Manufactured by BIHOS S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INBRUSH - Primary ID 08033480009074
Device Regulatory Overview
The INBRUSH (Model/Catalog Number: BSP10000M) is a medical device manufactured by BIHOS S.r.l.. This product is indexed under FDA Product Code / Category Classification R01058099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BSP10000M
- Product Code / EMDN
- R01058099
- Device Name
- SPAZZOLINO
- Database Sync Date
- 2026-08-09 16:48:48
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 INBRUSH?
The registered manufacturer of record for INBRUSH is BIHOS S.r.l..
What is the Primary UDI-DI identifier for INBRUSH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033480009074.
What classification code is assigned to this device?
This device is registered under product classification code R01058099.
Similar Classification Devices (R01058099)
Other Devices by BIHOS S.r.l.
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