Taiwan FDA registration 1a17e47ddaf25787e669f5015cad4790
"GUENTER BISSINGER" Manual surgical instrument for general use (Non-Sterile)
TW: "君特比辛格" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·GUENTER BISSINGER MEDIZINTECHNIK GMBH·Registered Apr 21, 2016 – Apr 21, 2021ExpiredRegistration details
- Analysis ID
- 1a17e47ddaf25787e669f5015cad4790
- License Form
- Ministry of Health Medical Device Import No. 016426
- Customs Code
- DHA09401642604
Company information
- Manufacturer
- GUENTER BISSINGER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SMARTECH 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
- Apr 21, 2016
- Expiry Date
- Apr 21, 2021
About this record
Access comprehensive regulatory information for "GUENTER BISSINGER" 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 1a17e47ddaf25787e669f5015cad4790 and manufactured by GUENTER BISSINGER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..
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