Taiwan FDA registration 9f3858461e3d6317ab120da490e67e30
“MJK” Manual Surgical Instrument for General Use(Non-Sterile)
TW: “姆傑克”一般手術用手動器械(未滅菌)
Taiwan·Risk Class 1·MD·MJK INSTRUMENTS·Registered Feb 18, 2019 – Feb 18, 2024ExpiredRegistration details
- Analysis ID
- 9f3858461e3d6317ab120da490e67e30
- License Form
- Ministry of Health Medical Device Import No. 020102
- Customs Code
- DHA09402010206
Company information
- Manufacturer
- MJK INSTRUMENTS
- Manufacturer Country
- France
- Authorized Representative
- Senka 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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 18, 2019
- Expiry Date
- Feb 18, 2024
About this record
Access comprehensive regulatory information for “MJK” 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 9f3858461e3d6317ab120da490e67e30 and manufactured by MJK INSTRUMENTS. The authorized representative in Taiwan is Senka Co., Ltd..
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