Philippines FDA registration CMDR-2021-00117

BD VENFLON™ PRO SAFETY / BD INSTAFLASH™ NEEDLE TECHNOLOGY NEEDLE PROTECTED IV CANNULA (E-BEAM STERILIZED)

Philippines flagPhilippines·Becton Dickinson Infusion Therapy AB - Helsingborg, Sweden mfd. By: BD Medical (S) Pte. Ltd. - Tuas Avenue 2, Singapore·Singapore·Issued July 02, 2021 – July 02, 2026
Device information
Product Name
BD VENFLON™ PRO SAFETY / BD INSTAFLASH™ NEEDLE TECHNOLOGY NEEDLE PROTECTED IV CANNULA (E-BEAM STERILIZED)
Registration Number
CMDR-2021-00117
Manufacturer details
Country of Origin
Singapore
Importer & distribution
Importer/Distributor
KSM Healthcare, Inc.
Registration dates
Issuance Date
July 02, 2021
Expiry Date
July 02, 2026
About this record

Access comprehensive regulatory information for BD VENFLON™ PRO SAFETY / BD INSTAFLASH™ NEEDLE TECHNOLOGY NEEDLE PROTECTED IV CANNULA (E-BEAM STERILIZED) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2021-00117 and manufactured by Becton Dickinson Infusion Therapy AB - Helsingborg, Sweden mfd. By: BD Medical (S) Pte. Ltd. - Tuas Avenue 2, Singapore in Singapore. The device was registered on July 02, 2021.

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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