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Vitros Immunodiagnostic Products Anti-HBE Reagent Pack - FDA Registration RR-1721

Access comprehensive regulatory information for Vitros Immunodiagnostic Products Anti-HBE Reagent Pack in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number RR-1721 and manufactured by Ortho-Clinical Diagnostics Felindre Meadows, Pencoed, Bridgend, CF35 5PZ, United Kingdom in United Kingdom. The device was registered on May 09, 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
RR-1721
Vitros Immunodiagnostic Products Anti-HBE Reagent Pack
Registered medical device in Philippines
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Device Information
Product Name
Vitros Immunodiagnostic Products Anti-HBE Reagent Pack
Registration Number
RR-1721
Manufacturer Details
Importer & Distribution
Registration Dates
Issuance Date
May 09, 2023
Expiry Date
January 09, 2028