Taiwan FDA registration e3e4ecb2aae28f2b928f68d1da15a832
“IMDS” NHancer Guidewire Support Catheter
TW: “迎成”恩施導線支持微細導管
Taiwan·Risk Class 2·MD·IMDS Operations B.V.·Registered Oct 13, 2014 – Oct 13, 2019CancelledRegistration details
- Analysis ID
- e3e4ecb2aae28f2b928f68d1da15a832
- License Form
- Ministry of Health Medical Device Import No. 026584
- Customs Code
- DHA05602658408
Company information
- Manufacturer
- IMDS Operations B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 13, 2014
- Expiry Date
- Oct 13, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “IMDS” NHancer Guidewire Support Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3e4ecb2aae28f2b928f68d1da15a832 and manufactured by IMDS Operations B.V.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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