Taiwan FDA registration 72e27f78d2554fbb9f84cd3f6718f466
"Fuku Leimei" manual instrument for general surgery (not sterilized)
TW: “福雷明”一般手術用手動式器械（未滅菌）
Taiwan·Risk Class 1·HUAIAN FRIMEN CO., LTD·Registered Mar 30, 2010 – Mar 30, 2020CancelledRegistration details
- Analysis ID
- 72e27f78d2554fbb9f84cd3f6718f466
- Customs Code
- DHA04600089806
Company information
- Manufacturer
- HUAIAN FRIMEN CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- Shangqun Limited
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
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 30, 2010
- Expiry Date
- Mar 30, 2020
- Cancellation Date
- May 27, 2020
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Fuku Leimei" 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 72e27f78d2554fbb9f84cd3f6718f466 and manufactured by HUAIAN FRIMEN CO., LTD. The authorized representative in Taiwan is Shangqun Limited.
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