Taiwan FDA registration 48c78624423df142218ddc05e3e2e8dc

“STORZ MEDICAL” Extracorporeal shock wave Therapy System

TW: “斯拓茲”體外震波治療系統
Taiwan flagTaiwan·Risk Class 3·MD·Storz Medical AG·Registered May 22, 2018 – May 22, 2028Active
Registration details
Analysis ID
48c78624423df142218ddc05e3e2e8dc
License Form
Ministry of Health Medical Device Import No. 031091
Customs Code
DHA05603109105
Company information
Manufacturer
Storz Medical AG
Manufacturer Country
Switzerland
Authorized Representative
KINDMED CORPORATION
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order. New indications: as detailed as Chinese copy of the single approval. (The original copy of the original approved copy of the imitation slip and label approved in 108.7.13 shall be collected and invalidated). The following blanks.
Product Type (Level 1)
H Gastroenterology-urology devices
Product Type (Level 2)
H9999 Other
Import Information
Imported from abroad
Dates and status
Registration Date
May 22, 2018
Expiry Date
May 22, 2028
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About this record

Access comprehensive regulatory information for “STORZ MEDICAL” Extracorporeal 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 48c78624423df142218ddc05e3e2e8dc and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Storz Medical AG, and 2 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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