Taiwan FDA registration dba5fec5df315b5c1f9cbb97b6050135

"Meike" auditory evoked response tester and its accessories

TW: "美科"聽性誘發反應測試儀及其附件
Taiwan flagTaiwan·MAICO DIAGNOSTIC GMBH·Registered May 16, 2006 – May 16, 2011Cancelled
Registration details
Analysis ID
dba5fec5df315b5c1f9cbb97b6050135
Customs Code
DHA00601446007
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
Import Information
import
Dates and status
Registration Date
May 16, 2006
Expiry Date
May 16, 2011
Cancellation Date
Nov 23, 2012
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. 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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