Taiwan FDA registration 294e7f28e94f25627b1ea822e7e961a7
“MAICO” Tympanometer
TW: “麥科”聽阻檢查儀
Taiwan·Risk Class 2·MD·MAICO Diagnostics GmbH·Registered Dec 11, 2017 – Dec 11, 2027ActiveRegistration details
- Analysis ID
- 294e7f28e94f25627b1ea822e7e961a7
- License Form
- Ministry of Health Medical Device Import No. 030584
- Customs Code
- DHA05603058400
Company information
- Manufacturer
- MAICO Diagnostics GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- KING PAX TECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G1090 Hearing Impaired Tester
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 11, 2017
- Expiry Date
- Dec 11, 2027
About this record
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..
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