Taiwan FDA registration 77cfb5c9d48ad7ef972567a5413156ba
"Ai Iji" surgical manual instrument (unsterilized)
TW: “伊司愛”手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·ELECTRO SURGICAL INSTRUMENT CO.·Registered Mar 12, 2007 – Mar 12, 2022CancelledRegistration details
- Analysis ID
- 77cfb5c9d48ad7ef972567a5413156ba
- Customs Code
- DHA04400566607
Company information
- Manufacturer
- ELECTRO SURGICAL INSTRUMENT CO.
- Manufacturer Country
- United States
- Authorized Representative
- WELLONG INSTRUMENTS 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
- import
Dates and status
- Registration Date
- Mar 12, 2007
- Expiry Date
- Mar 12, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ai Iji" surgical manual instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77cfb5c9d48ad7ef972567a5413156ba and manufactured by ELECTRO SURGICAL INSTRUMENT CO.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..
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