Taiwan FDA registration f057a7c9331294ea2f53bbe5af5c8638
ISTAR PTCA BALLOON CATHETER
TW: 愛斯達氣球導管
Taiwan·Risk Class 2·MD·amg International GmbH·Registered Dec 22, 2018 – Dec 22, 2023ExpiredRegistration details
- Analysis ID
- f057a7c9331294ea2f53bbe5af5c8638
- License Form
- Ministry of Health Medical Device Import No. 031878
- Customs Code
- DHA05603187806
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)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 22, 2018
- Expiry Date
- Dec 22, 2023
About this record
Access comprehensive regulatory information for ISTAR PTCA BALLOON CATHETER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f057a7c9331294ea2f53bbe5af5c8638 and manufactured by amg International GmbH. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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