Taiwan FDA registration 704c2b2e963c26a27bbdf5deee929068
“Ditron” Manual Surgical Instrument for General Use (Non-Sterile)
TW: “東昇”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·DITRON DENTAL LTD.·Registered Jul 03, 2020 – Jul 03, 2025ExpiredRegistration details
- Analysis ID
- 704c2b2e963c26a27bbdf5deee929068
- License Form
- Ministry of Health Medical Device Import No. 021700
- Customs Code
- DHA09402170005
Company information
- Manufacturer
- DITRON DENTAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- TUNG SHENG MEDICAL 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
- Jul 03, 2020
- Expiry Date
- Jul 03, 2025
About this record
Access comprehensive regulatory information for “Ditron” 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 704c2b2e963c26a27bbdf5deee929068 and manufactured by DITRON DENTAL LTD.. The authorized representative in Taiwan is TUNG SHENG MEDICAL INC..
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