Taiwan FDA registration 52e3204144e37972c2d0e0b7255ffa56
“REDA” Manual surgical instrument for general use (Non-Sterile)
TW: “芮達”一般手術用手動式器械(未滅菌)
Taiwan·Risk Class 1·MD·REDA INSTRUMENTE GMBH·Registered Mar 29, 2021 – Mar 29, 2026ExpiredRegistration details
- Analysis ID
- 52e3204144e37972c2d0e0b7255ffa56
- License Form
- Ministry of Health Medical Device Import No. 022420
- Customs Code
- DHA09402242004
Company information
- Manufacturer
- REDA INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TAIWAN MEDICAL SUPPLY, INC.
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 29, 2021
- Expiry Date
- Mar 29, 2026
About this record
Access comprehensive regulatory information for “REDA” 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 52e3204144e37972c2d0e0b7255ffa56 and manufactured by REDA INSTRUMENTE GMBH. The authorized representative in Taiwan is TAIWAN MEDICAL SUPPLY, INC..
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