Eu Ivdr
Eu Ivd Class B
On The Market
🇨🇿 Czechia
RIA 17α-Hydroxyprogesterone
Devices (same UDI-DI)
1
Certificates
0
Countries
18
Notified Bodies
0
Basic Information
- Primary DI
- 15099590214715
- Basic UDI-DI Code
- 150995905IM14525M
- Reference
- IM1452
- Device Types
- None provided
- Regulation
- Eu Ivdr
- Classification
- Eu Ivd Class B
- Status
- On The Market
- Manufacturer
- IMMUNOTECH s.r.o.
Additional Description
RIA 17α-Hydroxyprogesterone is an in vitro diagnostic manual medical device intended to be used by healthcare professionals for the quantitative measurement of 17α-hydroxyprogesterone in human serum and plasma. Measurement of 17α-hydroxyprogesterone is intended to be used for differential diagnosis of hyperandrogenism and for diagnosis and monitoring of congenital adrenal hyperplasia in general population.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102050107 | 17 OH PROGESTERONE |
Available In Countries
🇦🇹 Austria
🇧🇪 Belgium
🇨🇾 Cyprus
🇨🇿 Czechia
🇩🇪 Germany
🇬🇷 Greece
🇪🇸 Spain
🇫🇷 France
🇭🇺 Hungary
🇮🇪 Ireland
🇮🇹 Italy
🇱🇮 Liechtenstein
🇱🇹 Lithuania
🇱🇺 Luxembourg
🇲🇹 Malta
🇵🇱 Poland
🇵🇹 Portugal
🇸🇰 Slovakia
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