Philippines FDA registration CMDR-2025-04128

Simplex® All-Silicone Duodenal Tube, NGT/Levin

Philippines·Ningbo Greatcare Trading Co., Ltd. - Unit 93, Building 12, No. 818, Qiming Road, Yinzhou, 315105 Ningbo, Zhejiang, China Mfd. By: Well Lead Medical Co., Ltd. - C-4 Jinhu Industrial Estate, Hualong, 511434 Panyu, Guangzhou, People's Republic of China·China·Issued March 12, 2025 – March 12, 2030

Device information

Product Name: Simplex® All-Silicone Duodenal Tube, NGT/Levin
Registration Number: CMDR-2025-04128

Manufacturer details

Manufacturer: Ningbo Greatcare Trading Co., Ltd. - Unit 93, Building 12, No. 818, Qiming Road, Yinzhou, 315105 Ningbo, Zhejiang, China Mfd. By: Well Lead Medical Co., Ltd. - C-4 Jinhu Industrial Estate, Hualong, 511434 Panyu, Guangzhou, People's Republic of China
Country of Origin: China

Importer & distribution

Importer/Distributor: Panamed Philippines, Inc.

Registration dates

Issuance Date: March 12, 2025
Expiry Date: March 12, 2030

About this record

Access comprehensive regulatory information for Simplex® All-Silicone Duodenal Tube, NGT/Levin in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04128 and manufactured by Ningbo Greatcare Trading Co., Ltd. - Unit 93, Building 12, No. 818, Qiming Road, Yinzhou, 315105 Ningbo, Zhejiang, China Mfd. By: Well Lead Medical Co., Ltd. - C-4 Jinhu Industrial Estate, Hualong, 511434 Panyu, Guangzhou, People's Republic of China in China. The device was registered on March 12, 2025.

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