Eu Ivdr
Eu Ivd Class B
On The Market
๐จ๐ฟ Czechia
Angiotensin I RIA KIT
Devices (same UDI-DI)
1
Certificates
0
Countries
19
Notified Bodies
0
Basic Information
- Primary DI
- 15099590219574
- Basic UDI-DI Code
- 150995905IM351868
- Reference
- IM3518
- Device Types
- None provided
- Regulation
- Eu Ivdr
- Classification
- Eu Ivd Class B
- Status
- On The Market
- Manufacturer
- IMMUNOTECH s.r.o.
Additional Description
Angiotensin I RIA KIT is an in vitro diagnostic manual medical device intended to be used by healthcare professionals for the quantitative measurement of plasma renin activity (PRA) in human plasma. Measurement of plasma renin activity is intended to be used as an aid in diagnosis and differential diagnosis of primary and secondary hyperaldosteronism and hypoaldosteronism in general population.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102060202 | ANGIOTENSIN I / II |
Available In Countries
๐ฆ๐น Austria
๐ง๐ช Belgium
๐จ๐พ Cyprus
๐จ๐ฟ Czechia
๐ฉ๐ช Germany
๐ฉ๐ฐ Denmark
๐ฌ๐ท Greece
๐ช๐ธ Spain
๐ซ๐ท France
๐ญ๐บ Hungary
๐ฎ๐ช Ireland
๐ฎ๐น Italy
๐ฑ๐ฎ Liechtenstein
๐ฑ๐น Lithuania
๐ฑ๐บ Luxembourg
๐ฒ๐น Malta
๐ต๐ฑ Poland
๐ต๐น Portugal
๐ธ๐ฐ Slovakia
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