eudamed_udi
Primary ID: 08435804520713
master diagnóstica (UDI 08435804520713)
Manufactured by VITRO, S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for master diagnóstica - Primary ID 08435804520713
Device Regulatory Overview
The master diagnóstica (Model/Catalog Number: MAD-011892QEVS) is a medical device manufactured by VITRO, S.A.. This product is indexed under FDA Product Code / Category Classification W01030799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MAD-011892QEVS
- Product Code / EMDN
- W01030799
- Device Name
- Proteinase K (RTU)
- Database Sync Date
- 2026-08-09 18:01:27
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 master diagnóstica?
The registered manufacturer of record for master diagnóstica is VITRO, S.A..
What is the Primary UDI-DI identifier for master diagnóstica?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435804520713.
What classification code is assigned to this device?
This device is registered under product classification code W01030799.
Similar Classification Devices (W01030799)
Other Devices by VITRO, S.A.
Programmatic Export
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