Eu Ivdr
Eu Ivd Class B
On The Market
🇨🇿 Czechia
ACTIVE® Androstenedione RIA
Devices (same UDI-DI)
1
Certificates
0
Countries
17
Notified Bodies
0
Basic Information
- Primary DI
- 15099590211516
- Basic UDI-DI Code
- 150995905DSL3800FG
- Reference
- DSL3800
- Device Types
- None provided
- Regulation
- Eu Ivdr
- Classification
- Eu Ivd Class B
- Status
- On The Market
- Manufacturer
- IMMUNOTECH s.r.o.
Additional Description
ACTIVE® Androstenedione RIA is an in vitro diagnostic manual medical device intended to be used by healthcare professionals for the quantitative measurement of androstenedione in human serum and plasma. Measurement of androstenedione is intended to be used for diagnosis and differential diagnosis of hyperandrogenism and for diagnosis and monitoring of congenital adrenal hyperplasia in general population.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102050101 | ANDROSTENEDIONE |
Available In Countries
🇦🇹 Austria
🇧🇪 Belgium
🇨🇾 Cyprus
🇨🇿 Czechia
🇩🇪 Germany
🇬🇷 Greece
🇪🇸 Spain
🇫🇷 France
🇭🇺 Hungary
🇮🇪 Ireland
🇮🇹 Italy
🇱🇮 Liechtenstein
🇱🇺 Luxembourg
🇲🇹 Malta
🇵🇱 Poland
🇵🇹 Portugal
🇸🇰 Slovakia
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