Taiwan FDA registration 84e1b08592e16d6ccad9e674d5dd242e
“Asahi” Neurovascular Guide Wire
TW: “朝日”神經血管導引線
Taiwan·Risk Class 2·MD·ASAHI INTECC CO., LTD. SETO FACTORY·Registered May 09, 2014 – May 09, 2019CancelledRegistration details
- Analysis ID
- 84e1b08592e16d6ccad9e674d5dd242e
- License Form
- Ministry of Health Medical Device Import No. 026144
- Customs Code
- DHA05602614406
Company information
- Manufacturer
- ASAHI INTECC CO., LTD. SETO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 09, 2014
- Expiry Date
- May 09, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Asahi” Neurovascular Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84e1b08592e16d6ccad9e674d5dd242e and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is HI-CLEARANCE INC..
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