eudamed_udi
Primary ID: 08053847360082
MIZAR (UDI 08053847360082)
Manufactured by GINEVRI srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MIZAR - Primary ID 08053847360082
Device Regulatory Overview
The MIZAR (Model/Catalog Number: 8089) is a medical device manufactured by GINEVRI srl. This product is indexed under FDA Product Code / Category Classification Z12080401,Z12080407 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8089
- Product Code / EMDN
- Z12080401,Z12080407
- Device Name
- MIZAR
- Database Sync Date
- 2026-08-09 16:29:48
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 MIZAR?
The registered manufacturer of record for MIZAR is GINEVRI srl.
What is the Primary UDI-DI identifier for MIZAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053847360082.
What classification code is assigned to this device?
This device is registered under product classification code Z12080401,Z12080407.
Similar Classification Devices (Z12080401,Z12080407)
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