Taiwan FDA registration e335db0185fb0f9982e3ab7c74069c87
"Kikosei" uterine device (unsterilized)
TW: “喜兒生”子宮刮器 （未滅菌）
Taiwan·Risk Class 1·HSI ERH SHENG ENTERPRISE CO., LTD.·Registered Aug 31, 2006 – Aug 31, 2016CancelledRegistration details
- Analysis ID
- e335db0185fb0f9982e3ab7c74069c87
Company information
- Manufacturer
- HSI ERH SHENG ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HSI ERH SHENG ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for Obstetrics and Gynecology (L.4530)".
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.4530 婦產科專用手動器械
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 31, 2006
- Expiry Date
- Aug 31, 2016
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kikosei" uterine device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e335db0185fb0f9982e3ab7c74069c87 and manufactured by HSI ERH SHENG ENTERPRISE CO., LTD.. The authorized representative in Taiwan is HSI ERH SHENG ENTERPRISE CO., LTD..
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