Taiwan FDA registration 9c26e60d8d5eec1a1cd57fe94685f30d
"Baylis" Toronto atrial diaphragm catheter
TW: “貝利斯”多倫多房中膈導管
Taiwan·Risk Class 2·BAYLIS MEDICAL COMPANY INC.·Registered Dec 31, 2008 – Dec 31, 2013CancelledRegistration details
- Analysis ID
- 9c26e60d8d5eec1a1cd57fe94685f30d
- Customs Code
- DHA00601954501
Company information
- Manufacturer
- BAYLIS MEDICAL COMPANY INC.
- Manufacturer Country
- Canada
- Authorized Representative
- CHINA SPRING TRADING 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
- Product Type (Level 2)
- E.5175 Panectomy Conduit
- Import Information
- import
Dates and status
- Registration Date
- Dec 31, 2008
- Expiry Date
- Dec 31, 2013
- Cancellation Date
- Aug 05, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baylis" Toronto atrial diaphragm catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c26e60d8d5eec1a1cd57fe94685f30d and manufactured by BAYLIS MEDICAL COMPANY INC.. The authorized representative in Taiwan is CHINA SPRING TRADING 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