Taiwan FDA registration 8f7cbed7aa890a345de128bb9040f3c4
"Goodkey" angiogram catheter
TW: "固特克"血管攝影導管
Registration details
- Analysis ID
- 8f7cbed7aa890a345de128bb9040f3c4
- Customs Code
- DHA00600886304
Company information
- Manufacturer
- GOODTEC CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- CHINA HOSMED INTERNATIONAL INC.
Product details
- Product Type (Level 1)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 1998
- Expiry Date
- Oct 01, 2018
- 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 "Goodkey" angiogram catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f7cbed7aa890a345de128bb9040f3c4 and manufactured by GOODTEC CO., LTD.. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices