Philippines FDA registration DVR-5856

Tracheostomy Tube Cuff (Sterile)

Philippines·Kenxin International Company Ltd. - Room 714,West Tower No. 140 West Zhongshan Avenue, Tianhe District, Huagang Office Building, Guangzhou City, Guangdong Province, China·China·Issued September 19, 2024 – April 11, 2029

Device information

Product Name: Tracheostomy Tube Cuff (Sterile)
Registration Number: DVR-5856

Manufacturer details

Manufacturer: Kenxin International Company Ltd. - Room 714,West Tower No. 140 West Zhongshan Avenue, Tianhe District, Huagang Office Building, Guangzhou City, Guangdong Province, China
Country of Origin: China

Importer & distribution

Importer/Distributor: Indoplas Philippines Inc

Registration dates

Issuance Date: September 19, 2024
Expiry Date: April 11, 2029

About this record

Access comprehensive regulatory information for Tracheostomy Tube Cuff (Sterile) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5856 and manufactured by Kenxin International Company Ltd. - Room 714,West Tower No. 140 West Zhongshan Avenue, Tianhe District, Huagang Office Building, Guangzhou City, Guangdong Province, China in China. The device was registered on September 19, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Indoplas 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.