Philippines FDA registration CMDR-2025-03932

Canack PVC Manual Resuscitator

Philippines·Ningbo Luke Medical Devices CO., Ltd. No. 178 Gujiayan, Qishan Village, Yangming Street, Yuyao City, Zhejiang 315400, China·China·Issued February 24, 2025 – February 24, 2030

Device information

Product Name: Canack PVC Manual Resuscitator
Registration Number: CMDR-2025-03932

Manufacturer details

Manufacturer: Ningbo Luke Medical Devices CO., Ltd. No. 178 Gujiayan, Qishan Village, Yangming Street, Yuyao City, Zhejiang 315400, China
Country of Origin: China

Importer & distribution

Importer/Distributor: Josmef Medical Corporation

Registration dates

Issuance Date: February 24, 2025
Expiry Date: February 24, 2030

About this record

Access comprehensive regulatory information for Canack PVC Manual Resuscitator in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03932 and manufactured by Ningbo Luke Medical Devices CO., Ltd. No. 178 Gujiayan, Qishan Village, Yangming Street, Yuyao City, Zhejiang 315400, China in China. The device was registered on February 24, 2025.

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.