Eu Mdr Eu Md Class 2a On The Market ๐Ÿ‡ง๐Ÿ‡ช Belgium

ArtiQ.PFT

ArtiQ NV ยท ๐Ÿ‡ง๐Ÿ‡ช Belgium
Devices (same UDI-DI)
2
Certificates
0
Countries
20
Notified Bodies
0

Basic Information

Primary DI
05419980057600
Basic UDI-DI Code
54199800576ArtiQ.PFT1HQ
Reference
N/A
Device Types
None provided
Regulation
Eu Mdr
Classification
Eu Md Class 2a
Status
On The Market
Manufacturer
ArtiQ NV

Additional Description

The intended purpose of ArtiQ.PFT is to provide automated interpretation of pulmonary function tests (PFTs) to assist physicians in the diagnosis and follow-up of respiratory diseases. It is a software as medical device with no graphical user interface that can be used through an application programming interface (API) for the generation of ArtiQ.PFT reports. These reports are meant to supplement, and by no means substitute, any initial report(s) generated by PFT devices, and are not meant to be used as a replacement of the medical practitioner's interpretation.

CND Nomenclature Codes

Code Description
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER

Available In Countries

๐Ÿ‡ฆ๐Ÿ‡น Austria ๐Ÿ‡ง๐Ÿ‡ช Belgium ๐Ÿ‡จ๐Ÿ‡พ Cyprus ๐Ÿ‡จ๐Ÿ‡ฟ Czechia ๐Ÿ‡ฉ๐Ÿ‡ช Germany ๐Ÿ‡ฉ๐Ÿ‡ฐ Denmark ๐Ÿ‡ช๐Ÿ‡ธ Spain ๐Ÿ‡ซ๐Ÿ‡ฎ Finland ๐Ÿ‡ซ๐Ÿ‡ท France ๐Ÿ‡ฎ๐Ÿ‡ช Ireland ๐Ÿ‡ฎ๐Ÿ‡น Italy ๐Ÿ‡ฑ๐Ÿ‡ฎ Liechtenstein ๐Ÿ‡ฑ๐Ÿ‡บ Luxembourg ๐Ÿ‡ฒ๐Ÿ‡น Malta ๐Ÿ‡ณ๐Ÿ‡ฑ Netherlands ๐Ÿ‡ณ๐Ÿ‡ด Norway ๐Ÿ‡ต๐Ÿ‡ฑ Poland ๐Ÿ‡ท๐Ÿ‡ด Romania ๐Ÿ‡ธ๐Ÿ‡ช Sweden ๐Ÿ‡ฌ๐Ÿ‡ง United Kingdom

Related Devices

The Basic UDI-DI associated with this device has 2 devices in total. Below are some other devices sharing the same Basic UDI-DI.

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