Taiwan FDA registration 025b1179e08b67f3698f40223c9f8b3f
"Jiacheng" poured into the filter tube group (sterilized)
TW: “佳承” 灌入過濾管組 (滅菌)
Taiwan·Risk Class 1·Jiacheng Seiko Co., Ltd. second factory·Registered Oct 11, 2012 – Oct 11, 2017CancelledRegistration details
- Analysis ID
- 025b1179e08b67f3698f40223c9f8b3f
Company information
- Manufacturer
- Jiacheng Seiko Co., Ltd. second factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Jiacheng Seiko Co., Ltd. second factory
Product details
- Intended Use
- Limited to the first level recognition range of laparoscopic perfusion device (L.1730) for the management of medical devices.
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1730 腹腔鏡灌入器
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Oct 11, 2012
- Expiry Date
- Oct 11, 2017
- Cancellation Date
- Dec 05, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jiacheng" poured into the filter tube group (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 025b1179e08b67f3698f40223c9f8b3f and manufactured by Jiacheng Seiko Co., Ltd. second factory. The authorized representative in Taiwan is Jiacheng Seiko Co., Ltd. second factory.
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