GUDIDData
eudamed_udi Primary ID: 08908015304279

TRUPCR® Respiratory Pathogen Panel Kit (UDI 08908015304279)

Manufactured by 3B BlackBio Dx Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRUPCR® Respiratory Pathogen Panel Kit - Primary ID 08908015304279

Device Regulatory Overview

The TRUPCR® Respiratory Pathogen Panel Kit (Model/Catalog Number: 3B288) is a medical device manufactured by 3B BlackBio Dx Limited. This product is indexed under FDA Product Code / Category Classification W0105900102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3B288
Product Code / EMDN
W0105900102
Device Name
TRUPCR® Respiratory Pathogen Panel Kit
Database Sync Date
2026-08-09 16:59:17

Full Regulatory Attributes

🔒 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 TRUPCR® Respiratory Pathogen Panel Kit?

The registered manufacturer of record for TRUPCR® Respiratory Pathogen Panel Kit is 3B BlackBio Dx Limited.

What is the Primary UDI-DI identifier for TRUPCR® Respiratory Pathogen Panel Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08908015304279.

What classification code is assigned to this device?

This device is registered under product classification code W0105900102.

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