Taiwan FDA registration 2e742fec977acc11eac9766449420a2c

"Siemens" extracorporeal shock wave lithotripsy

TW: “西門子”體外震波碎石機
Taiwan flagTaiwan·Risk Class 2·SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP·Registered Apr 23, 2008 – Apr 23, 2018Cancelled
Registration details
Analysis ID
2e742fec977acc11eac9766449420a2c
Customs Code
DHAS0601881405
Company information
Manufacturer Country
Germany
Authorized Representative
SIEMENS LIMITED
Product details
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.5990 體外震波碎石器
Import Information
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
Registration Date
Apr 23, 2008
Expiry Date
Apr 23, 2018
Cancellation Date
May 12, 2017
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

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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