Taiwan FDA registration 1bafcbac845d4f49c627eade9f7c4fcd
"Hailier" radio frequency electric cauter
TW: “海利爾”射頻電燒灼器
Taiwan·Risk Class 2·Stellartech Research Corporation;; HALYARD HEALTH, INC.·Registered May 05, 2017 – May 05, 2022CancelledRegistration details
- Analysis ID
- 1bafcbac845d4f49c627eade9f7c4fcd
- Customs Code
- DHA05602971400
Company information
- Manufacturer Country
- United States
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4400 Shot Cutout Generator
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- May 05, 2017
- Expiry Date
- May 05, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hailier" radio frequency electric cauter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1bafcbac845d4f49c627eade9f7c4fcd and manufactured by Stellartech Research Corporation;; HALYARD HEALTH, INC.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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