Taiwan FDA registration 8f7ee0c4f510f41f796be5fe3a53b407
“Bard” Proxis Ureteral Access Sheath
TW: “巴德”波瑟斯輸尿管通路導尿管鞘
Taiwan·Risk Class 2·MD·C.R. BARD, INC.·Registered Mar 24, 2019 – Mar 24, 2024ExpiredRegistration details
- Analysis ID
- 8f7ee0c4f510f41f796be5fe3a53b407
- License Form
- Ministry of Health Medical Device Import No. 032348
- Customs Code
- DHA05603234808
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)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 24, 2019
- Expiry Date
- Mar 24, 2024
About this record
Access comprehensive regulatory information for “Bard” Proxis Ureteral Access Sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f7ee0c4f510f41f796be5fe3a53b407 and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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