Philippines FDA registration MDR-10591

ALARIS™ GP VOLUMETRIC PUMP TRANSFUSION/BLOOD SET, 2 SPIKE, 200µm FILTER

Philippines flagPhilippines·Becton Dickinson Holdings Pte. Ltd. - Singapore mfd. By: Carefusion BH 335 d.o.o. Cazin, Bosnia & Herzegovina For: BD Switzerland Sarl - Eysins, Switzerland·Switzerland·Issued November 06, 2020 – November 06, 2021
Device information
Product Name
ALARIS™ GP VOLUMETRIC PUMP TRANSFUSION/BLOOD SET, 2 SPIKE, 200µm FILTER
Registration Number
MDR-10591
Manufacturer details
Country of Origin
Switzerland
Importer & distribution
Importer/Distributor
KSM Healthcare, Inc.
Registration dates
Issuance Date
November 06, 2020
Expiry Date
November 06, 2021
About this record

Access comprehensive regulatory information for ALARIS™ GP VOLUMETRIC PUMP TRANSFUSION/BLOOD SET, 2 SPIKE, 200µm FILTER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10591 and manufactured by Becton Dickinson Holdings Pte. Ltd. - Singapore mfd. By: Carefusion BH 335 d.o.o. Cazin, Bosnia & Herzegovina For: BD Switzerland Sarl - Eysins, Switzerland in Switzerland. The device was registered on November 06, 2020.

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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