eudamed_udi
Primary ID: 08057680910756
CLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B (UDI 08057680910756)
Manufactured by Clonit srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B - Primary ID 08057680910756
Device Regulatory Overview
The CLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B (Model/Catalog Number: OP02012-48) is a medical device manufactured by Clonit srl. This product is indexed under FDA Product Code / Category Classification W0105900101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OP02012-48
- Product Code / EMDN
- W0105900101
- Device Name
- CLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B
- Database Sync Date
- 2026-08-09 17:37:31
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 CLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B?
The registered manufacturer of record for CLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B is Clonit srl.
What is the Primary UDI-DI identifier for CLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057680910756.
What classification code is assigned to this device?
This device is registered under product classification code W0105900101.
Similar Classification Devices (W0105900101)
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