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"Meike" auditory evoked response tester and its accessories - Taiwan Registration dba5fec5df315b5c1f9cbb97b6050135

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. is registered under number dba5fec5df315b5c1f9cbb97b6050135 and manufactured by MAICO DIAGNOSTIC 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 Diagnostics 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.

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dba5fec5df315b5c1f9cbb97b6050135
Registration Details
Taiwan FDA Registration: dba5fec5df315b5c1f9cbb97b6050135
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Device Details

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

Registration Details

dba5fec5df315b5c1f9cbb97b6050135

DHA00601446007

Company Information

Germany

Product Details

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

K Neuroscience

import

Dates and Status

May 16, 2006

May 16, 2011

Nov 23, 2012

Cancellation Information

Logged out

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