Taiwan FDA registration a0567f5889c73474e561e2a3705fc8bb
“ADEOR” Manual surgical instrument for general use (Non-Sterile)
TW: “艾德爾”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·ADEOR MEDICAL AG·Registered Jan 08, 2021 – Jan 08, 2026ExpiredRegistration details
- Analysis ID
- a0567f5889c73474e561e2a3705fc8bb
- License Form
- Ministry of Health Medical Device Import No. 022237
- Customs Code
- DHA09402223700
Company information
- Manufacturer
- ADEOR MEDICAL AG
- Manufacturer Country
- Germany
- Authorized Representative
- Shiang Tai Medical Instructment 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
- Jan 08, 2021
- Expiry Date
- Jan 08, 2026
About this record
Access comprehensive regulatory information for “ADEOR” 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 a0567f5889c73474e561e2a3705fc8bb and manufactured by ADEOR MEDICAL AG. The authorized representative in Taiwan is Shiang Tai Medical Instructment CO., LTD..
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