eudamed_udi
Primary ID: 08057680911289
Duplica BLOOD DNA Kit (UDI 08057680911289)
Manufactured by Clonit srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Duplica BLOOD DNA Kit - Primary ID 08057680911289
Device Regulatory Overview
The Duplica BLOOD DNA Kit (Model/Catalog Number: EDI002250) 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
- EDI002250
- Product Code / EMDN
- W0105900101
- Device Name
- Duplica BLOOD DNA Kit
- Database Sync Date
- 2026-08-09 17:55:00
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Duplica BLOOD DNA Kit?
The registered manufacturer of record for Duplica BLOOD DNA Kit is Clonit srl.
What is the Primary UDI-DI identifier for Duplica BLOOD DNA Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057680911289.
What classification code is assigned to this device?
This device is registered under product classification code W0105900101.
Similar Classification Devices (W0105900101)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint