Philippines FDA registration MDR-10114A

CANACK 2-WAY SILICONE FOLEY CATHETER

Philippines·Ningbo Luke Medical Devices Co., Ltd.·China·Issued July 30, 2020 – July 30, 2021

Device information

Product Name: CANACK 2-WAY SILICONE FOLEY CATHETER
Registration Number: MDR-10114A

Manufacturer details

Manufacturer: Ningbo Luke Medical Devices Co., Ltd.
Country of Origin: China

Importer & distribution

Importer/Distributor: Josmef Medical Corporation

Registration dates

Issuance Date: July 30, 2020
Expiry Date: July 30, 2021

About this record

Access comprehensive regulatory information for CANACK 2-WAY SILICONE FOLEY CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10114A and manufactured by Ningbo Luke Medical Devices Co., Ltd. in China. The device was registered on July 30, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Josmef Medical Corporation), 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.