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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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QMAPP — 4 UDI-DI variants, MDR (Fysicon B.V.)

MD Atlas
Fysicon B.V.

Data from EUDAMED, last updated May 30, 2026

QMAPP

8719689142QMAPPQ8

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Fysicon B.V.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8719689142QMAPPQ8
Device name: QMAPP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: Fysicon B.V.
SRN: NL-MF-000002694
Country: Netherlands
Email: info@fysicon.com
Phone: +31 412 65 33 33

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JQBX0J0P2RZ5V12QCMF34XJ4

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

QMAPP GO08719689142162
QMAPP HEMO08719689142124
QMAPP HEMO LT08719689142131
QMAPP PCM08719689142179