Taiwan FDA registration 13adc7795e1f00603f89f2db3df579f8
“Bard” Totalis Flexible Endo Kit
TW: “巴德”同達力斯可彎曲式泌尿科內視鏡套件
Taiwan·Risk Class 2·MD·C.R. BARD, INC.·Registered Jan 26, 2017 – Jan 26, 2022ExpiredRegistration details
- Analysis ID
- 13adc7795e1f00603f89f2db3df579f8
- License Form
- Ministry of Health Medical Device Import No. 029355
- Customs Code
- DHA05602935508
Company information
- Manufacturer
- C.R. BARD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Jan 26, 2017
- Expiry Date
- Jan 26, 2022
About this record
Access comprehensive regulatory information for “Bard” Totalis Flexible 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 13adc7795e1f00603f89f2db3df579f8 and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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