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"Siemens" extracorporeal shock wave lithotripsy - Taiwan Registration 2e742fec977acc11eac9766449420a2c

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 2e742fec977acc11eac9766449420a2c and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Siemens Healthcare GmbH, X-Ray Products (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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2e742fec977acc11eac9766449420a2c
Registration Details
Taiwan FDA Registration: 2e742fec977acc11eac9766449420a2c
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Device Details

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

Registration Details

2e742fec977acc11eac9766449420a2c

DHAS0601881405

Company Information

Product Details

H Gastroenterology and urology

H.5990 ้ซ”ๅค–้œ‡ๆณข็ขŽ็Ÿณๅ™จ

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Apr 23, 2008

Apr 23, 2018

May 12, 2017

Cancellation Information

Logged out

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