Taiwan FDA registration b80c859e7b3a153ea3e598447006331d
"Renqi" pneumoperitoneum needle
TW: “仁齊”氣腹針
Taiwan·Risk Class 2·TOP-BOUND ENTERPRISE CO., LTD.·Registered May 07, 2010 – May 07, 2015CancelledRegistration details
- Analysis ID
- b80c859e7b3a153ea3e598447006331d
- Customs Code
- DHY00500293801
Company information
- Manufacturer
- TOP-BOUND ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TOP-BOUND ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1720 Gynecology and gynecologic laparoscopes and their appendages
- Import Information
- Domestic
Dates and status
- Registration Date
- May 07, 2010
- Expiry Date
- May 07, 2015
- 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 "Renqi" pneumoperitoneum needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b80c859e7b3a153ea3e598447006331d and manufactured by TOP-BOUND ENTERPRISE CO., LTD.. The authorized representative in Taiwan is TOP-BOUND ENTERPRISE CO., LTD..
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