Taiwan FDA registration 76dec997c85632f5b91223cb93ab3926
Arthos Pico Stent Implantation System
TW: 阿受斯皮可冠狀動脈支架系統
Taiwan·Risk Class 3·MD·amg International GmbH·Registered Jan 23, 2018 – Jan 23, 2023ExpiredRegistration details
- Analysis ID
- 76dec997c85632f5b91223cb93ab3926
- License Form
- Ministry of Health Medical Device Import No. 030712
- Customs Code
- DHA05603071206
Company information
- Manufacturer
- amg International GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 23, 2018
- Expiry Date
- Jan 23, 2023
About this record
Access comprehensive regulatory information for Arthos Pico Stent Implantation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 76dec997c85632f5b91223cb93ab3926 and manufactured by amg International GmbH. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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