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“MAICO” Tympanometer - Taiwan Registration 294e7f28e94f25627b1ea822e7e961a7

Access comprehensive regulatory information for “MAICO” Tympanometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 294e7f28e94f25627b1ea822e7e961a7 and manufactured by MAICO Diagnostics GmbH. The authorized representative in Taiwan is KING PAX TECHNOLOGY 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.

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294e7f28e94f25627b1ea822e7e961a7
Registration Details
Taiwan FDA Registration: 294e7f28e94f25627b1ea822e7e961a7
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Device Details

“MAICO” Tympanometer
TW: “麥科”聽阻檢查儀
Risk Class 2
MD

Registration Details

294e7f28e94f25627b1ea822e7e961a7

Ministry of Health Medical Device Import No. 030584

DHA05603058400

Company Information

Germany

Product Details

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

G ENT device

G1090 Hearing Impaired Tester

Imported from abroad

Dates and Status

Dec 11, 2017

Dec 11, 2027