Taiwan FDA registration 3673511d8a4e3e21e93077d4564710d6
"Yuka" manual instrument for general surgery (not sterilized)
TW: “友華”一般手術用手動式器械（未滅菌）
Taiwan·Risk Class 1·Dayi Medical Instrument Factory·Registered Jan 05, 2010 – Jan 05, 2015CancelledRegistration details
- Analysis ID
- 3673511d8a4e3e21e93077d4564710d6
Company information
- Manufacturer
- Dayi Medical Instrument Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ORIENT EUROPHARMA 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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jan 05, 2010
- Expiry Date
- Jan 05, 2015
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Yuka" 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 3673511d8a4e3e21e93077d4564710d6 and manufactured by Dayi Medical Instrument Factory. The authorized representative in Taiwan is ORIENT EUROPHARMA CO., LTD..
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