Taiwan FDA registration 82dee84e558cf5c6a937cc55453e27f5
“SANUWAVE” dermaPACE Therapeutic Shock Wave System
TW: “索寧衛”得瑪貝司皮膚科震波治療系統
Taiwan·Risk Class 2·MD·SANUWAVE, Inc.·Registered Dec 06, 2022 – Dec 06, 2027ActiveRegistration details
- Analysis ID
- 82dee84e558cf5c6a937cc55453e27f5
- License Form
- Ministry of Health Medical Device Import No. 035942
- Customs Code
- DHA05603594209
Company information
- Manufacturer
- SANUWAVE, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Rhythm Medical Ltd.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4685 Extracorporeal shock wave therapy equipment for chronic wounds
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 06, 2022
- Expiry Date
- Dec 06, 2027
About this record
Access comprehensive regulatory information for “SANUWAVE” dermaPACE Therapeutic Shock Wave System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82dee84e558cf5c6a937cc55453e27f5 and manufactured by SANUWAVE, Inc.. The authorized representative in Taiwan is Rhythm Medical Ltd..
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