Eu Ivdr Eu Ivd Class B On The Market

IDS ACTH N

Devices (same UDI-DI)
3
Certificates
0
Countries
32
Notified Bodies
0

Basic Information

Primary DI
05060169695566
Basic UDI-DI Code
5060169695566YM
Reference
IS-4500N
Device Types
None provided
Regulation
Eu Ivdr
Classification
Eu Ivd Class B
Status
On The Market

Additional Description

The IDS iSYS ACTH assay is an in vitro diagnostic device intended for the quantitative determination of ACTH in human plasma on the IDS system. Results are to be used in conjunction with other clinical and laboratory data for the assessment of pituitary and adrenal gland function, the differential diagnosis of hyper- and hypo-cortisolism, as well as the evaluation of causes of endocrine hypertension.

CND Nomenclature Codes

Code Description
W0102060299 RENAL METABOLISM TESTS - OTHER

Available In Countries

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇾 Cyprus 🇨🇿 Czechia 🇩🇪 Germany 🇩🇰 Denmark 🇪🇪 Estonia 🇬🇷 Greece 🇪🇸 Spain 🇫🇮 Finland 🇫🇷 France 🇭🇷 Croatia 🇭🇺 Hungary 🇮🇪 Ireland 🇮🇸 Iceland 🇮🇹 Italy 🇱🇮 Liechtenstein 🇱🇹 Lithuania 🇱🇺 Luxembourg 🇱🇻 Latvia 🇲🇹 Malta 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇪 Sweden 🇸🇮 Slovenia 🇸🇰 Slovakia 🇹🇷 Türkiye 🇬🇧 United Kingdom

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