Taiwan FDA registration 31df9f47a81d04842babf482c825627c
"Bayer" Pyrok Thrombosis Removal Kit
TW: “拜耳”派若克血栓清除套組
Taiwan·Risk Class 2·Bayer Medical Care Inc.·Registered Apr 14, 2009 – Apr 14, 2019CancelledRegistration details
- Analysis ID
- 31df9f47a81d04842babf482c825627c
- Customs Code
- DHA00601978001
Company information
- Manufacturer
- Bayer Medical Care Inc.
- Manufacturer Country
- United States
- Authorized Representative
- WATTCAN INSTRUMENTS 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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- Apr 14, 2009
- Expiry Date
- Apr 14, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Bayer" Pyrok Thrombosis Removal Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 31df9f47a81d04842babf482c825627c and manufactured by Bayer Medical Care Inc.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS 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