eudamed_udi
Primary ID: 08059304340000
Unspecified Brand (UDI 08059304340000)
Manufactured by Visia Lab 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 08059304340000
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 49218) is a medical device manufactured by Visia Lab S.r.l.. This product is indexed under FDA Product Code / Category Classification W02079082 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 49218
- Product Code / EMDN
- W02079082
- Device Name
- ZENIT HEP2 CLASSIFIER
- Database Sync Date
- 2026-08-09 16:47:30
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 Visia Lab 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 08059304340000.
What classification code is assigned to this device?
This device is registered under product classification code W02079082.
Similar Classification Devices (W02079082)
Other Devices by Visia Lab S.r.l.
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