Taiwan FDA registration 479e60f911ea0590cc32e211636a801c
"Arno" epithelical sheath guide set
TW: “亞諾”皮膜鞘導引器組
Taiwan·Risk Class 2·ARROW INTERNATIONAL INC.·Registered Jul 10, 2007 – Jul 10, 2012CancelledRegistration details
- Analysis ID
- 479e60f911ea0590cc32e211636a801c
- Customs Code
- DHA00601815601
Company information
- Manufacturer
- ARROW INTERNATIONAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- CEMMA MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Jul 10, 2007
- Expiry Date
- Jul 10, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Arno" epithelical sheath guide set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 479e60f911ea0590cc32e211636a801c and manufactured by ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..
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