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BD Alaris™ Infusion Burette Set - FDA Registration MDR-04675

Access comprehensive regulatory information for BD Alaris™ Infusion Burette Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04675 and manufactured by BD Holdings Singapore Pte. Ltd. Mfd By: Sistemas Medicos Alaris S.A. De C.V. - Baja California, Mexico for BD Switzerland Sarl in Mexico. The device was registered on December 13, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (KSM Healthcare, 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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MDR-04675
BD Alaris™ Infusion Burette Set
Registered medical device in Philippines
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Device Information
Product Name
BD Alaris™ Infusion Burette Set
Registration Number
MDR-04675
Importer & Distribution
Importer/Distributor
KSM Healthcare, Inc.
Registration Dates
Issuance Date
December 13, 2022
Expiry Date
August 16, 2027