GUDIDData
eudamed_udi Primary ID: 08908007989897

Trueprep AUTO Universal Cartridge Based Sample Prep Kit (UDI 08908007989897)

Manufactured by Molbio Diagnostics Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Trueprep AUTO Universal Cartridge Based Sample Prep Kit - Primary ID 08908007989897

Device Regulatory Overview

The Trueprep AUTO Universal Cartridge Based Sample Prep Kit (Model/Catalog Number: 60203AR50) is a medical device manufactured by Molbio Diagnostics Limited. This product is indexed under FDA Product Code / Category Classification W0105900101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
60203AR50
Product Code / EMDN
W0105900101
Device Name
Trueprepยฎ AUTO Universal Cartridge Based Sample Prep Kit
Database Sync Date
2026-08-09 16:30:17

Full Regulatory Attributes

๐Ÿ”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Trueprep AUTO Universal Cartridge Based Sample Prep Kit?

The registered manufacturer of record for Trueprep AUTO Universal Cartridge Based Sample Prep Kit is Molbio Diagnostics Limited.

What is the Primary UDI-DI identifier for Trueprep AUTO Universal Cartridge Based Sample Prep Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08908007989897.

What classification code is assigned to this device?

This device is registered under product classification code W0105900101.

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