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BD Neoflon IV Cannula-Sterile - FDA Registration MDR-00045

Access comprehensive regulatory information for BD Neoflon IV Cannula-Sterile in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00045 and manufactured by Becton Dickinson Holdings Pte. Ltd. Singapore Mfd By: Becton Dickinson Medical (S) Pte. Ltd. - 30 Tuas Avenue 2, Singapore Mfd. By: Becton Dickinson Infusion Therapy AB - Helsingborg, Sweden in Singapore. The device was registered on November 14, 2023.

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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Singapore
MDR-00045
BD Neoflon IV Cannula-Sterile
Registered medical device in Philippines
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Device Information
Product Name
BD Neoflon IV Cannula-Sterile
Registration Number
MDR-00045
Importer & Distribution
Importer/Distributor
KSM Healthcare, Inc.
Registration Dates
Issuance Date
November 14, 2023
Expiry Date
July 11, 2028