Taiwan FDA registration de3a2babf47a30a107cb3dcaa1f5d153
“Sutter”Manual surgical instruments for general use (Non-Sterile)
TW: “修特”一般手術用手動式器械(未滅菌)
Taiwan·Risk Class 1·MD·SUTTER MEDIZINTECHNIK GMBH·Registered Nov 15, 2013 – Nov 15, 2023ExpiredRegistration details
- Analysis ID
- de3a2babf47a30a107cb3dcaa1f5d153
- License Form
- Ministry of Health Medical Device Import No. 013594
- Customs Code
- DHA09401359400
Company information
- Manufacturer
- SUTTER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HIGH TOP MEDICAL 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
- Nov 15, 2013
- Expiry Date
- Nov 15, 2023
About this record
Access comprehensive regulatory information for “Sutter”Manual surgical instruments 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 de3a2babf47a30a107cb3dcaa1f5d153 and manufactured by SUTTER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..
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