Taiwan FDA registration 251910e61174a0553225080dbd92e1d0
“Sanuwave” orthoPACE Shock Wave System
TW: “索寧衛”骨震波治療系統
Taiwan·Risk Class 3·MD·SANUWAVE, Inc.·Registered Dec 08, 2018 – Dec 08, 2023ExpiredRegistration details
- Analysis ID
- 251910e61174a0553225080dbd92e1d0
- License Form
- Ministry of Health Medical Device Import No. 031917
- Customs Code
- DHA05603191703
Company information
- Manufacturer
- SANUWAVE, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- LITHO MED TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N0001 Extracorporeal shock wave system for orthopedics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 08, 2018
- Expiry Date
- Dec 08, 2023
About this record
Access comprehensive regulatory information for “Sanuwave” orthoPACE Shock Wave System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 251910e61174a0553225080dbd92e1d0 and manufactured by SANUWAVE, Inc.. The authorized representative in Taiwan is LITHO MED TRADING CO., LTD..
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