Taiwan FDA registration 3e58604c53a5b73b201e9023eb82e94d
“Storz Medical” MASTERPULS ONE Shock Wave Therapy System
TW: “斯拓茲”麥斯波萬震波治療系統
Taiwan·Risk Class 3·MD·Storz Medical AG·Registered Dec 07, 2022 – Dec 07, 2027ActiveRegistration details
- Analysis ID
- 3e58604c53a5b73b201e9023eb82e94d
- License Form
- Ministry of Health Medical Device Import No. 035943
- Customs Code
- DHA05603594301
Company information
- Manufacturer
- Storz Medical AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- KINDMED CORPORATION
Product details
- Intended Use
- -肩關節慢性鈣化性或非鈣化性肌腱炎 (Chronic tendinitis of the shoulder)-慢性筋肌膜炎疼痛 (Chronic myofascial pain)-慢性足底筋膜炎 (Chronic plantar fasciitis)-慢性肘外上髁炎 (Chronic lateral epicondylitis)
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N0001 Extracorporeal shock wave system for orthopedics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 07, 2022
- Expiry Date
- Dec 07, 2027
About this record
Access comprehensive regulatory information for “Storz Medical” MASTERPULS ONE Shock Wave Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3e58604c53a5b73b201e9023eb82e94d and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.
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