Taiwan FDA registration f12d3fd247f6f96a69a981256b925ddd
"Rikijin" manual instrument for general surgery (not sterilized)
TW: "力仁" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·Liren Equipment Factory Co., Ltd·Registered Jan 16, 2015 – Jan 16, 2020CancelledRegistration details
- Analysis ID
- f12d3fd247f6f96a69a981256b925ddd
Company information
- Manufacturer
- Liren Equipment Factory Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Liren Equipment Factory 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 General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 16, 2015
- Expiry Date
- Jan 16, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rikijin" manual instrument for general surgery (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f12d3fd247f6f96a69a981256b925ddd and manufactured by Liren Equipment Factory Co., Ltd. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.
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