Philippines FDA registration CMDR-2025-04319

BeneVision N19

Name: BeneVision N19 — Philippines FDA registration CMDR-2025-04319
Creator: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Keywords: BeneVision N19, CMDR-2025-04319, Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Respicare Enterprises, Incorporated, China, Philippines FDA registration

PhilippinesShenzhen Mindray Bio-Medical Electronics Co., Ltd.ChinaIssued April 22, 2025 – April 22, 2030

VerifiedFDA Philippines · official registry

Device information

Product Name: BeneVision N19
Registration Number: CMDR-2025-04319

Manufacturer details

Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country of Origin: China

Importer & distribution

Importer/Distributor: Respicare Enterprises, Incorporated

Registration dates

Issuance Date: April 22, 2025
Expiry Date: April 22, 2030

About this record

Access comprehensive regulatory information for BeneVision N19 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04319 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. in China. The device was registered on April 22, 2025.

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