Philippines FDA registration RR-1720

VITROS IMMUNODIAGNOSTIC PRODUCTS HBeAg REAGENT PACK

Philippines flagPhilippines·Ortho-Clinical Diagnostics·United Kingdom·Issued February 12, 2018 – January 09, 2023
Device information
Product Name
VITROS IMMUNODIAGNOSTIC PRODUCTS HBeAg REAGENT PACK
Registration Number
RR-1720
Manufacturer details
Country of Origin
United Kingdom
Importer & distribution
Registration dates
Issuance Date
February 12, 2018
Expiry Date
January 09, 2023
About this record

Access comprehensive regulatory information for VITROS IMMUNODIAGNOSTIC PRODUCTS HBeAg REAGENT PACK in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number RR-1720 and manufactured by Ortho-Clinical Diagnostics in United Kingdom. The device was registered on February 12, 2018.

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.

Free DatabasePowered by Pure Global AIFDA Official DataUnited Kingdom