Pure Global

"Meike" auditory evoked response tester and its accessories - Taiwan Registration af66c08c0f606bd702463a9a89c161ce

Access comprehensive regulatory information for "Meike" auditory evoked response tester and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number af66c08c0f606bd702463a9a89c161ce and manufactured by MAICO Diagnostics GmbH. The authorized representative in Taiwan is RONAMAC INTERNATIONAL CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAICO DIAGNOSTIC GMBH, and 1 recent registrations in the same category. 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
1 Competitors
1 Recent Registrations
af66c08c0f606bd702463a9a89c161ce
Registration Details
Taiwan FDA Registration: af66c08c0f606bd702463a9a89c161ce
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Meike" auditory evoked response tester and its accessories
TW: โ€œ็พŽ็ง‘โ€่ฝๆ€ง่ช˜็™ผๅๆ‡‰ๆธฌ่ฉฆๅ„€ๅŠๅ…ถ้…ไปถ
Risk Class 2
Cancelled

Registration Details

af66c08c0f606bd702463a9a89c161ce

DHA00602313204

Company Information

Germany

Product Details

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

K Neuroscience

K.1900 ่ช˜็™ผๅๆ‡‰่ฒๅˆบๆฟ€ๅ™จ

import

Dates and Status

Dec 20, 2011

Dec 20, 2021

Aug 15, 2023

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ

Companies Making Similar Products
Top companies providing products similar to ""Meike" auditory evoked response tester and its accessories"