Taiwan FDA registration f4fb39d5e70a212f65be3f8259c55e2b
"Ampli" hearing impaired tester and its accessories
TW: “安普力”聽阻檢查儀及其配件
Taiwan·Risk Class 2·AMPLIVOX LTD.·Registered Jul 25, 2012 – Jul 25, 2022CancelledRegistration details
- Analysis ID
- f4fb39d5e70a212f65be3f8259c55e2b
- Customs Code
- DHA00602371706
Company information
- Manufacturer
- AMPLIVOX LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- RONAMAC INTERNATIONAL CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.1090 Auditory Resistance Checker
- Import Information
- import
Dates and status
- Registration Date
- Jul 25, 2012
- Expiry Date
- Jul 25, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ampli" hearing impaired 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 f4fb39d5e70a212f65be3f8259c55e2b and manufactured by AMPLIVOX LTD.. The authorized representative in Taiwan is RONAMAC INTERNATIONAL CORP..
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