Philippines FDA registration MDR-10111
RENASENZ AV FISTULA NEEDLE
Philippines·Jiangxi Hongda Medical Equipment Group Ltd.·China·Issued July 30, 2020 – July 30, 2021Device information
- Product Name
- RENASENZ AV FISTULA NEEDLE
- Registration Number
- MDR-10111
Manufacturer details
- Manufacturer
- Jiangxi Hongda Medical Equipment Group Ltd.
- Country of Origin
- China
Importer & distribution
- Importer/Distributor
- Panamed Philippines Inc.
Registration dates
- Issuance Date
- July 30, 2020
- Expiry Date
- July 30, 2021
About this record
Access comprehensive regulatory information for RENASENZ AV FISTULA NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10111 and manufactured by Jiangxi Hongda Medical Equipment Group Ltd. in China. The device was registered on July 30, 2020.
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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