Taiwan FDA registration 65ffb6c27d9263d5ab6397e288341e16
"Bard" Anjie adjustable single-cut suspension
TW: “巴德”安潔調整型單切口懸帶
Taiwan·Risk Class 2·C.R. BARD, INC.·Registered May 24, 2011 – May 24, 2021CancelledRegistration details
- Analysis ID
- 65ffb6c27d9263d5ab6397e288341e16
- Customs Code
- DHA00602241804
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)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- import
Dates and status
- Registration Date
- May 24, 2011
- Expiry Date
- May 24, 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" Anjie adjustable single-cut suspension in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 65ffb6c27d9263d5ab6397e288341e16 and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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