Pure Global

BD Venflon™ I IV Cannula BD Instaflash™ Needle Technology BD Luer-Lok™ - FDA Registration CMDR-2025-05041

Access comprehensive regulatory information for BD Venflon™ I IV Cannula BD Instaflash™ Needle Technology BD Luer-Lok™ in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05041 and manufactured by Becton Dickinson Holdings Pte. Ltd.- 2 International Business Park Road, The Strategy #08-08, Singapore 609930 Mfd. by: Becton Dickinson India Pvt. Ltd.- Plot No. 1 Sector 3, IMT, Bawal, District Rewari- 123 501, Haryana, India For: Becton Dickinson Infusion Therapy Systems Inc.- 9450 South State Sandy, Utah 84070, USA in Singapore. The device was registered on July 11, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Getz Bros. 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 Database
Powered by Pure Global AI
FDA Official Data
Singapore
CMDR-2025-05041
BD Venflon™ I IV Cannula BD Instaflash™ Needle Technology BD Luer-Lok™
Registered medical device in Philippines
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Importer & Distribution
Importer/Distributor
Getz Bros. Philippines, Inc.
Registration Dates
Issuance Date
July 11, 2025
Expiry Date
July 11, 2031