Taiwan FDA registration bcf779ffb2b94a45540d4d7858f41532
"Bard" vena cava filter
TW: “巴德”腔靜脈過濾器
Taiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.·Registered Nov 25, 2009 – Nov 25, 2014CancelledRegistration details
- Analysis ID
- bcf779ffb2b94a45540d4d7858f41532
- Customs Code
- DHA00602043609
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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3375 Cardiovascular vascular spillers
- Import Information
- import
Dates and status
- Registration Date
- Nov 25, 2009
- Expiry Date
- Nov 25, 2014
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bard" vena cava filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bcf779ffb2b94a45540d4d7858f41532 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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