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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Qassay Lateral Flow Reader DUAL — 3 UDI-DI variants, IVDR

MD Atlas
P4Q Health S.L.U.

Data from EUDAMED, last updated May 23, 2026

Qassay Lateral Flow Reader DUAL

8445982Q1A-DUO-USBZM

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: P4Q Health S.L.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8445982Q1A-DUO-USBZM
Device name: Qassay Lateral Flow Reader DUAL
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: P4Q Health S.L.U.
SRN: ES-MF-000039526
Country: Spain
Email: sales@p4q.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HTMFNXBAND2KQGBTPRTW90EF

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

iREAD08445982000037
Q1A-DUO-USB 08445982000075
Q1A-DUO-USB-00208445982000181