Taiwan FDA registration 240b3d177fbc8aa32e60ddcc887cc66a

“Storz” Masterpuls Shock Wave Therapy System

TW: “思拓”邁氏波震波治療系統
Taiwan flagTaiwan·Risk Class 3·MD·STORZ MEDICAL AG·Registered Sep 13, 2013 – Sep 13, 2018Cancelled
Registration details
Analysis ID
240b3d177fbc8aa32e60ddcc887cc66a
License Form
Ministry of Health Medical Device Import No. 025412
Customs Code
DHA05602541200
Company information
Manufacturer
STORZ MEDICAL AG
Manufacturer Country
Switzerland
Authorized Representative
SHAWHAN BIOMEDICAL CO., LTD.
Product details
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
Sep 13, 2013
Expiry Date
Sep 13, 2018
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for “Storz” Masterpuls 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 240b3d177fbc8aa32e60ddcc887cc66a and manufactured by STORZ MEDICAL AG. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Storz Medical AG, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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