Taiwan FDA registration af66c08c0f606bd702463a9a89c161ce

"Meike" auditory evoked response tester and its accessories

TW: “美科”聽性誘發反應測試儀及其配件
Taiwan flagTaiwan·Risk Class 2·MAICO Diagnostics GmbH·Registered Dec 20, 2011 – Dec 20, 2021Cancelled
Registration details
Analysis ID
af66c08c0f606bd702463a9a89c161ce
Customs Code
DHA00602313204
Company information
Manufacturer Country
Germany
Authorized Representative
RONAMAC INTERNATIONAL CORP.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
K Neuroscience
Product Type (Level 2)
K.1900 誘發反應聲刺激器
Import Information
import
Dates and status
Registration Date
Dec 20, 2011
Expiry Date
Dec 20, 2021
Cancellation Date
Aug 15, 2023
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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..

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