Philippines FDA registration IVDR-00371
ORTHO BIOVUE SYSTEM REVERSE DILUENT CASSETTE
Philippines·Ortho-Clinical Diagnostics·USA·Issued January 30, 2019 – January 30, 2020Device information
- Product Name
- ORTHO BIOVUE SYSTEM REVERSE DILUENT CASSETTE
- Registration Number
- IVDR-00371
Manufacturer details
- Manufacturer
- Ortho-Clinical Diagnostics
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Ortho-Clinical Diagnostics Philippines Inc.
Registration dates
- Issuance Date
- January 30, 2019
- Expiry Date
- January 30, 2020
About this record
Access comprehensive regulatory information for ORTHO BIOVUE SYSTEM REVERSE DILUENT CASSETTE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00371 and manufactured by Ortho-Clinical Diagnostics in USA. The device was registered on January 30, 2019.
This page provides complete registration details including manufacturer information, importer/distributor details (Ortho-Clinical Diagnostics Philippines Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.
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