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ALARIS™ GP VOLUMETRIC PUMP ALARIS™ SAFETY CLAMP SMARTSITE™ NEEDLE-FREE SYSTEM, INFUSION SET, NO FILTER - FDA Registration MDR-10105

Access comprehensive regulatory information for ALARIS™ GP VOLUMETRIC PUMP ALARIS™ SAFETY CLAMP SMARTSITE™ NEEDLE-FREE SYSTEM, INFUSION SET, NO FILTER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10105 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 August 02, 2021.

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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Switzerland
MDR-10105
ALARIS™ GP VOLUMETRIC PUMP ALARIS™ SAFETY CLAMP SMARTSITE™ NEEDLE-FREE SYSTEM, INFUSION SET, NO FILTER
Registered medical device in Philippines
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Device Information
Product Name
ALARIS™ GP VOLUMETRIC PUMP ALARIS™ SAFETY CLAMP SMARTSITE™ NEEDLE-FREE SYSTEM, INFUSION SET, NO FILTER
Registration Number
MDR-10105
Importer & Distribution
Importer/Distributor
KSM Healthcare, Inc.
Registration Dates
Issuance Date
August 02, 2021
Expiry Date
July 30, 2026