Philippines FDA registration MDR-03899

Quadrox-I Adult HMO70000 + VHK 71000 Oxygenator with Venous Hardshell Cardiotomy Reservoir

Philippines flagPhilippines·Getinge Southeast Asia Pte. Ltd. - Singapore Mfd. By: Maquet Cardiopulmonary Medical Teknik San Tic. Ltd. - Sti-Antalya, Turkey For: Maquet Cardiopulmonary GmbH - Rastatt, Germany·Singapore·Issued September 02, 2022 – January 22, 2027
Device information
Product Name
Quadrox-I Adult HMO70000 + VHK 71000 Oxygenator with Venous Hardshell Cardiotomy Reservoir
Registration Number
MDR-03899
Manufacturer details
Country of Origin
Singapore
Importer & distribution
Registration dates
Issuance Date
September 02, 2022
Expiry Date
January 22, 2027
About this record

Access comprehensive regulatory information for Quadrox-I Adult HMO70000 + VHK 71000 Oxygenator with Venous Hardshell Cardiotomy Reservoir in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-03899 and manufactured by Getinge Southeast Asia Pte. Ltd. - Singapore Mfd. By: Maquet Cardiopulmonary Medical Teknik San Tic. Ltd. - Sti-Antalya, Turkey For: Maquet Cardiopulmonary GmbH - Rastatt, Germany in Singapore. The device was registered on September 02, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Medtronix Medical Supplies & Equipment), 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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