Taiwan FDA registration 11ed293c4ac0e91fa98059cd905c3a7e
“ASAHI” SHEATHLESS EAUCATH PTCA GUIDING CATHETER
TW: “朝日”無需導引鞘水漾經皮冠狀動脈成型術導引導管
Registration details
- Analysis ID
- 11ed293c4ac0e91fa98059cd905c3a7e
- License Form
- Ministry of Health Medical Device Import No. 031825
- Customs Code
- DHA05603182501
Company information
- Manufacturer
- ASAHI INTECC(THAILAND) CO., LTD
- Manufacturer Country
- Thailand
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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
- Oct 18, 2018
- Expiry Date
- Oct 18, 2023
About this record
Access comprehensive regulatory information for “ASAHI” SHEATHLESS EAUCATH PTCA GUIDING CATHETER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11ed293c4ac0e91fa98059cd905c3a7e and manufactured by ASAHI INTECC(THAILAND) CO., LTD. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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