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Ortho® Antibody Enhancement Solution - FDA Registration IVDR-00188

Access comprehensive regulatory information for Ortho® Antibody Enhancement Solution in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00188 and manufactured by Ortho-Clinical Diagnostics Felindre Meadows Pencoed, Bridgend, United Kingdom Mfd. By: Ortho-Clinical Diagnostics Inc. 1001 US Highway 202, Raritan, New Jearsey, USA in United Kingdom. The device was registered on February 07, 2023.

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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United Kingdom
IVDR-00188
Ortho® Antibody Enhancement Solution
Registered medical device in Philippines
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Device Information
Product Name
Ortho® Antibody Enhancement Solution
Registration Number
IVDR-00188
Importer & Distribution
Registration Dates
Issuance Date
February 07, 2023
Expiry Date
April 05, 2027