GUDIDData
eudamed_udi Primary ID: 00842768003653

Dade PFA Collagen/EPI Test Cartridge (UDI 00842768003653)

Manufactured by Siemens Healthcare Diagnostics Products GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dade PFA Collagen/EPI Test Cartridge - Primary ID 00842768003653

Device Regulatory Overview

The Dade PFA Collagen/EPI Test Cartridge (Model/Catalog Number: 10445696) is a medical device manufactured by Siemens Healthcare Diagnostics Products GmbH. This product is indexed under FDA Product Code / Category Classification W0103020401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10445696
Product Code / EMDN
W0103020401
Device Name
IVDR_27_MAR EB_B_REAG_PFA_Coll_ADP_EPI
Database Sync Date
2026-08-09 16:30:14

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 Dade PFA Collagen/EPI Test Cartridge?

The registered manufacturer of record for Dade PFA Collagen/EPI Test Cartridge is Siemens Healthcare Diagnostics Products GmbH.

What is the Primary UDI-DI identifier for Dade PFA Collagen/EPI Test Cartridge?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842768003653.

What classification code is assigned to this device?

This device is registered under product classification code W0103020401.

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