Taiwan FDA registration ef562a8a4a1dde54e9cb77aaebb2fa8e
“Vycor” Manual Surgical Instrument for General Use (Non-Sterile)
TW: “博科”一般手術用手動式器械（未滅菌）
Taiwan·Risk Class 1·MD·VYCOR MEDICAL INC.·Registered Mar 21, 2014 – Mar 21, 2024ExpiredRegistration details
- Analysis ID
- ef562a8a4a1dde54e9cb77aaebb2fa8e
- License Form
- Ministry of Health Medical Device Import No. 013979
- Customs Code
- DHA09401397904
Company information
- Manufacturer
- VYCOR MEDICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- MATECH HEALTHCARE CORPORATION
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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 21, 2014
- Expiry Date
- Mar 21, 2024
About this record
Access comprehensive regulatory information for “Vycor” Manual Surgical Instrument for General Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef562a8a4a1dde54e9cb77aaebb2fa8e and manufactured by VYCOR MEDICAL INC.. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.
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