Philippines FDA registration IVDR-00369

ORTHO ANTIBODY ENHANCEMENT SOLUTION IN VITRO DIAGNOSTIC SOLUTION

Philippines flagPhilippines·Ortho-Clinical Diagnostics·USA·Issued January 30, 2019 – January 30, 2020
Device information
Product Name
ORTHO ANTIBODY ENHANCEMENT SOLUTION IN VITRO DIAGNOSTIC SOLUTION
Registration Number
IVDR-00369
Manufacturer details
Country of Origin
USA
Importer & distribution
Registration dates
Issuance Date
January 30, 2019
Expiry Date
January 30, 2020
About this record

Access comprehensive regulatory information for ORTHO ANTIBODY ENHANCEMENT SOLUTION IN VITRO DIAGNOSTIC SOLUTION in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00369 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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