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"DIVA" Medical image communication device (Non-Sterile) - Taiwan Registration 2f43378c995f0e51de0f3d27b7ca1e24

Access comprehensive regulatory information for "DIVA" Medical image communication device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2f43378c995f0e51de0f3d27b7ca1e24 and manufactured by DIVA LABORATORIES, LTD.. The authorized representative in Taiwan is DIVA LABORATORIES, LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2f43378c995f0e51de0f3d27b7ca1e24
Registration Details
Taiwan FDA Registration: 2f43378c995f0e51de0f3d27b7ca1e24
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Device Details

"DIVA" Medical image communication device (Non-Sterile)
TW: "้ˆบ็ทฏ" ้†ซๅญธๅฝฑๅƒๅ‚ณ่ผธ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2f43378c995f0e51de0f3d27b7ca1e24

Ministry of Health Medical Device Manufacturing No. 006634

Company Information

Taiwan, Province of China

Product Details

Limited to the first-level recognition range of medical image transmission devices (P.2020) of the Measures for the Administration of Medical Devices.

P Devices for radiology

P2020 Medical Image Transmission Device

Produced in Taiwan, China

Dates and Status

Mar 16, 2017

Mar 16, 2022