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"Siemens" extracorporeal shock wave lithotripsy - Taiwan Registration fbc700687b8623182ca1c672f2143939

Access comprehensive regulatory information for "Siemens" extracorporeal shock wave lithotripsy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fbc700687b8623182ca1c672f2143939 and manufactured by Siemens Healthcare GmbH, X-Ray Products (XP). The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP, 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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fbc700687b8623182ca1c672f2143939
Registration Details
Taiwan FDA Registration: fbc700687b8623182ca1c672f2143939
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Device Details

"Siemens" extracorporeal shock wave lithotripsy
TW: "่ฅฟ้–€ๅญ"้ซ”ๅค–้œ‡ๆณข็ขŽ็ŸณๆฉŸ
Risk Class 2
Cancelled

Registration Details

fbc700687b8623182ca1c672f2143939

DHAS0601396208

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Feb 09, 2006

Feb 09, 2021

Aug 04, 2023

Cancellation Information

Logged out

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