Taiwan FDA registration 681ab420bec02afab7cfce39329715d8
“Bard” Totalis Rigid Endo Kit
TW: “巴德”同達力斯硬質泌尿科內視鏡套件
Taiwan·Risk Class 2·MD·C.R. BARD, INC.·Registered Aug 19, 2016 – Aug 19, 2021CancelledRegistration details
- Analysis ID
- 681ab420bec02afab7cfce39329715d8
- License Form
- Ministry of Health Medical Device Import No. 028740
- Customs Code
- DHA05602874006
Company information
- Manufacturer
- C.R. BARD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H4620 Ureteral stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 19, 2016
- Expiry Date
- Aug 19, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Bard” Totalis Rigid Endo Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 681ab420bec02afab7cfce39329715d8 and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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