Philippines FDA registration CMDR-2025-03758B

Canack Endotracheal Tube Reinforced, uncuffed

Philippines·Ningbo Luke Medical Devices Co., Ltd.·China·Issued January 31, 2025 – January 31, 2030

Device information

Product Name: Canack Endotracheal Tube Reinforced, uncuffed
Registration Number: CMDR-2025-03758B

Manufacturer details

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

Importer & distribution

Importer/Distributor: Josmef Enterprises

Registration dates

Issuance Date: January 31, 2025
Expiry Date: January 31, 2030

About this record

Access comprehensive regulatory information for Canack Endotracheal Tube Reinforced, uncuffed in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03758B and manufactured by Ningbo Luke Medical Devices Co., Ltd. in China. The device was registered on January 31, 2025.

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