Philippines FDA registration CMDR-2025-03758A

Canack Endotracheal Tube

Name: Canack Endotracheal Tube — Philippines FDA registration CMDR-2025-03758A
Creator: Ningbo Luke Medical Devices Co., Ltd.
Keywords: Canack Endotracheal Tube, CMDR-2025-03758A, Ningbo Luke Medical Devices Co., Ltd., Josmef Enterprises, China, Philippines FDA registration

PhilippinesNingbo Luke Medical Devices Co., Ltd.ChinaIssued January 31, 2025 – January 31, 2030

VerifiedFDA Philippines · official registry

Device information

Product Name: Canack Endotracheal Tube
Registration Number: CMDR-2025-03758A

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 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03758A 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.