Philippines FDA registration MDR-07812

INTRAPLAS NELATON CATHETER

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 June 26, 2025 – March 14, 2031

Device information

Product Name: INTRAPLAS NELATON CATHETER
Registration Number: MDR-07812

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: June 26, 2025
Expiry Date: March 14, 2031

About this record

Access comprehensive regulatory information for INTRAPLAS NELATON CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07812 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 June 26, 2025.

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.