VOLUMAT LINES VL TR12 - FDA Registration MDR-01373
Access comprehensive regulatory information for VOLUMAT LINES VL TR12 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01373 and manufactured by Fresenius Kabi Asia Pacific Ltd. in Germany. The device was registered on August 27, 2019.
This page provides complete registration details including manufacturer information, importer/distributor details (Fresenius Kabi 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.
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Germany
MDR-01373
VOLUMAT LINES VL TR12
Registered medical device in Philippines
Device Information
Product Name
VOLUMAT LINES VL TR12
Registration Number
MDR-01373
Manufacturer Details
Manufacturer
Fresenius Kabi Asia Pacific Ltd.Country of Origin
Germany
Importer & Distribution
Importer/Distributor
Fresenius Kabi Philippines, Inc.Registration Dates
Issuance Date
August 27, 2019
Expiry Date
July 23, 2024

