PAD BUFFER
- Risk class
- IV
- Product type
- In Vitro Diagnostic
- Brand name
- DIAGAST
- Commercial name
- 19-294 IVD Reagents/Kits, Immunohematology, Blood Pooling
- Analysis ID
- 6981cff8cc81d7f8279f48976542eb9d
- Registration date
- December 07, 2022
- Expiration date
- December 07, 2027
- Name
- DIAGAST
- City
- LOOS
- Country
- FRENCH
- Address
- 251 AVENUE EUGENE AVINNEE, 59120 LOOS- FRANCE
- Name
- DIAGAST
- Country
- FRENCH
- Address
- BARRIO JIPIJAPA STREET: ISLA FERNANDINA NO. N42-40 INTERSECCION ISLA TORTUGA
- Phone
- 2252800
THEY ARE USED IN ASSOCIATION WITH PAD® DEVICES AS AN ACTIVATION BUFFER. OF THE REAGENTS AND OF DISCLOSURE OF THE RESULTS, WHICH ALLOWS TO DETECT, FROM A SAMPLE OF WHOLE BLOOD OR RED BLOOD CONCENTRATE, A REACTION BETWEEN AN ERYTHROCYTE ANTIGEN AND AN ANTIBODY SPECIFICALLY DIRECTED AGAINST THIS ANTIGEN.
Access comprehensive regulatory information for PAD BUFFER in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 6981cff8cc81d7f8279f48976542eb9d and manufactured by DIAGAST. The device was registered on December 07, 2022.
This page provides complete registration details including product type (In Vitro Diagnostic), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.