Eu Ivdr
Eu Ivd Class C
On The Market
🇰🇷 South Korea
PROTIA Allergy-Q 128M
Devices (same UDI-DI)
1
Certificates
0
Countries
1
Notified Bodies
0
Basic Information
- Primary DI
- 08809446480658
- Basic UDI-DI Code
- 880944648ALM01HN
- Reference
- PALM0112
- Device Types
-
Single use
- Regulation
- Eu Ivdr
- Classification
- Eu Ivd Class C
- Status
- On The Market
- Manufacturer
- PROTIA Inc.
Additional Description
PROTIA Allergy-Q 128M is an in vitro diagnostic test in the semi-quantitative determination of allergen-specific IgE and quantitative detection of total IgE antibodies in human serum or plasma (anticoagulated with heparin or citrate) using immunoblotting technique.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W01020204 | IMMUNOGLOBULIN E - MONOTEST/PLURIRESULT-MULTI AG |
Available In Countries
🇹🇷 Türkiye
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd Class C) and regulation (EU IVDR).
CREATININE
Device
EU IVDR
·
Eu Ivd Class C
·Medicon Hellas SA·On the market·1 country
CREATININE
Device
EU IVDR
·
Eu Ivd Class C
·Medicon Hellas SA·On the market·1 country
MH Guide
Device
EU IVDR
·
Eu Ivd Class C
·Molecular Health GmbH·On the market·2 countries
CREATININE
Device
EU IVDR
·
Eu Ivd Class C
·Medicon Hellas SA·On the market·1 country
CREATININE
Device
EU IVDR
·
Eu Ivd Class C
·Medicon Hellas SA·On the market·1 country
CREATININE
Device
EU IVDR
·
Eu Ivd Class C
·Medicon Hellas SA·On the market·1 country