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SIMPLEX® Foley Catheter, 2-Way, with Stylet - FDA Registration MDR-05022 A

Access comprehensive regulatory information for SIMPLEX® Foley Catheter, 2-Way, with Stylet in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05022 A and manufactured by Fuzhou Kanglite Medical Apparatus Co., Ltd. - Room 02, No. 17 Floor West Jinyuan Plaza, No. 68, Guangda Road, Taijang, Fuzhou, 350005, Fujian, P.R. China in China. The device was registered on July 21, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Panamed 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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China
MDR-05022 A
SIMPLEX® Foley Catheter, 2-Way, with Stylet
Registered medical device in Philippines
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Device Information
Product Name
SIMPLEX® Foley Catheter, 2-Way, with Stylet
Registration Number
MDR-05022 A
Importer & Distribution
Importer/Distributor
Panamed Philippines Inc.
Registration Dates
Issuance Date
July 21, 2023
Expiry Date
January 09, 2028