Xpert ® Bladder Cancer Monitor
- Risk class
- III
- Product type
- In Vitro Diagnostic
- Brand name
- Xpert
- Commercial name
- 26-998.- Reagents/Kits for IVD Assays, Molecular Assay, Gene Expression
- Sterilization method
- METHODOLOGY: MOLECULAR DIAGNOSIS
- Analysis ID
- e6c779f29b3739062f58d0a81ff0eb98
- Registration date
- October 05, 2022
- Expiration date
- October 05, 2027
- Creation date
- May 10, 2022
- Name
- CEPHEID
- City
- SUNNYVALE, CA
- Country
- UNITED STATES
- Address
- 904, CARIBBEAN DRIVE - SUNNYVALE, CA 94089 - USA
- Name
- CEPHEID
- Country
- UNITED STATES
- Address
- TODOS LOS SANTOS # 201 AND AV. JORGE PEREZ CONCHA
- Phone
- 2610680
IT IS A DIAGNOSTIC TEST IN VITRO QUALITATIVE DESIGNED TO MONITOR BLADDER CANCER RELAPSE IN PREVIOUSLY OCCURRING PATIENTS DIAGNOSED WITH BLADDER CANCER.
Access comprehensive regulatory information for Xpert ® Bladder Cancer Monitor in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID e6c779f29b3739062f58d0a81ff0eb98 and manufactured by CEPHEID. The device was registered on October 05, 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.