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Covidien Kangaroo™ e-Pump Set with Flush Bag, Anti-Free Flow - FDA Registration CMDR-2025-04394

Access comprehensive regulatory information for Covidien Kangaroo™ e-Pump Set with Flush Bag, Anti-Free Flow in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04394 and manufactured by Cardinal Health 200, LLC 3651 Birchwood Drive Waukegan, IL 60085 USA Mfd By: Cardinal Health Costa Rica, S.A. Edificio B20, Calle #2, Zona Franca Coyol, Alajuela, Costa Rica For: Covidien llc - 15 Hampshire Street, Mansfield, MA 02048, USA in USA. The device was registered on May 06, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Lifelink, 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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CMDR-2025-04394
Covidien Kangaroo™ e-Pump Set with Flush Bag, Anti-Free Flow
Registered medical device in Philippines
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Device Information
Product Name
Covidien Kangaroo™ e-Pump Set with Flush Bag, Anti-Free Flow
Registration Number
CMDR-2025-04394
Importer & Distribution
Importer/Distributor
Lifelink, Inc.
Registration Dates
Issuance Date
May 06, 2025
Expiry Date
May 06, 2030