eudamed_udi
Primary ID: 08052107111532
BRUSH (UDI 08052107111532)
Manufactured by AK MEDICAL S.R.L. UNIPERSONALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BRUSH - Primary ID 08052107111532
Device Regulatory Overview
The BRUSH (Model/Catalog Number: CHTT-BR) is a medical device manufactured by AK MEDICAL S.R.L. UNIPERSONALE. This product is indexed under FDA Product Code / Category Classification R01058099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CHTT-BR
- Product Code / EMDN
- R01058099
- Device Name
- SPAZZOLINO PULIZIA CANNULE TRACHEO
- Database Sync Date
- 2026-08-09 16:50:33
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 BRUSH?
The registered manufacturer of record for BRUSH is AK MEDICAL S.R.L. UNIPERSONALE.
What is the Primary UDI-DI identifier for BRUSH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052107111532.
What classification code is assigned to this device?
This device is registered under product classification code R01058099.
Similar Classification Devices (R01058099)
Other Devices by AK MEDICAL S.R.L. UNIPERSONALE
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