Taiwan FDA registration 1d94af9c2c8558564ac0adc3d6e39bac
Siemens extracorporeal shock wave lithotripter
TW: 西門子 體外震波碎石機
Taiwan·SIEMENS AG·Registered Dec 19, 1987 – Dec 19, 1999CancelledRegistration details
- Analysis ID
- 1d94af9c2c8558564ac0adc3d6e39bac
- Customs Code
- DHA00600494400
Company information
- Manufacturer
- SIEMENS AG
- Manufacturer Country
- Germany
- Authorized Representative
- UNISON COMPANY LTD.
Product details
- Product Type (Level 1)
- 0900 Lithotripsy
- Import Information
- import
Dates and status
- Registration Date
- Dec 19, 1987
- Expiry Date
- Dec 19, 1999
- Cancellation Date
- Feb 22, 2000
Cancellation information
- Status
- Logged out
- Reason
- 逾期展延
About this record
Access comprehensive regulatory information for Siemens extracorporeal shock wave lithotripter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 1d94af9c2c8558564ac0adc3d6e39bac and manufactured by SIEMENS AG. The authorized representative in Taiwan is UNISON COMPANY LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices