eudamed_udi
Primary ID: 08059304700583
Unspecified Brand (UDI 08059304700583)
Manufactured by Titanox S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08059304700583
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: A1-091-626/LV) is a medical device manufactured by Titanox S.r.l.. This product is indexed under FDA Product Code / Category Classification S0199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A1-091-626/LV
- Product Code / EMDN
- S0199
- Device Name
- Aluminum containers with filter
- Database Sync Date
- 2026-08-09 16:46:25
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Titanox S.r.l..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08059304700583.
What classification code is assigned to this device?
This device is registered under product classification code S0199.
Similar Classification Devices (S0199)
Other Devices by Titanox S.r.l.
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