Pure Global

ROTALINK™ PLUS PRE-CONNECTED EXCHANGEABLE CATHETER AND BURR ADVANCING DEVICE - FDA Registration MDR-06802

Access comprehensive regulatory information for ROTALINK™ PLUS PRE-CONNECTED EXCHANGEABLE CATHETER AND BURR ADVANCING DEVICE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06802 and manufactured by Boston scientific corporation - 300 boston scientific way marlborough, MA 01721-1234 USA mfd by: Boston Scientific Limited - Business & Technology Park Model Farm Rd., Cork, Ireland in Ireland. The device was registered on May 14, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Boston Scientific 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
Ireland
MDR-06802
ROTALINK™ PLUS PRE-CONNECTED EXCHANGEABLE CATHETER AND BURR ADVANCING DEVICE
Registered medical device in Philippines
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Information
Product Name
ROTALINK™ PLUS PRE-CONNECTED EXCHANGEABLE CATHETER AND BURR ADVANCING DEVICE
Registration Number
MDR-06802
Importer & Distribution
Registration Dates
Issuance Date
May 14, 2025
Expiry Date
May 29, 2029