Pure Global

"Guise Ai" middle ear analyzer - Taiwan Registration 42141cba0c9c655fe0707a2a5b396cd9

Access comprehensive regulatory information for "Guise Ai" middle ear analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42141cba0c9c655fe0707a2a5b396cd9 and manufactured by DGS Diagnostics Sp. z o.o.;;DIAGNOSTIC GROUP LLC Doing Business As Grason-Stadler. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS CO., 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
42141cba0c9c655fe0707a2a5b396cd9
Registration Details
Taiwan FDA Registration: 42141cba0c9c655fe0707a2a5b396cd9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Guise Ai" middle ear analyzer
TW: โ€œๅ‰ๆ–ฏ่‰พโ€ ไธญ่€ณๅˆ†ๆžๅ„€
Risk Class 2

Registration Details

42141cba0c9c655fe0707a2a5b396cd9

DHA05602897000

Product Details

For details, it is Chinese approved copy of the imitation order.

G ENT Science

G.1090 Auditory Resistance Checker

import

Dates and Status

Nov 24, 2016

Nov 24, 2026