Taiwan FDA registration 05e7cb5e1fd35eee6dd7a8b20e552265
“Bard” Vacora Vacuum Assisted Biopsy System Accessories
TW: “巴德”維可拉真空輔助組織取樣系統配件
Taiwan·Risk Class 2·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Dec 26, 2016 – Dec 26, 2026ActiveRegistration details
- Analysis ID
- 05e7cb5e1fd35eee6dd7a8b20e552265
- License Form
- Ministry of Health Medical Device Import No. 029230
- Customs Code
- DHA05602923001
Company information
- Manufacturer
- BARD PERIPHERAL VASCULAR, 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)
- H1075 Gastroenterology - Urology biopsy instruments
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 26, 2016
- Expiry Date
- Dec 26, 2026
About this record
Access comprehensive regulatory information for “Bard” Vacora Vacuum Assisted Biopsy System Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05e7cb5e1fd35eee6dd7a8b20e552265 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE 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