Taiwan FDA registration f737010898ed2b9909fd878ad5096d0e
"Siemens" mobile digital X-ray machine
TW: "西門子" 移動式數位X光機
Taiwan·Risk Class 2·SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP;; SIEMENS, S.A.·Registered Mar 02, 2006 – Mar 02, 2016CancelledRegistration details
- Analysis ID
- f737010898ed2b9909fd878ad5096d0e
- Customs Code
- DHAS0601405506
Company information
- Manufacturer Country
- Spain;;Germany
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- 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
- Mar 02, 2006
- Expiry Date
- Mar 02, 2016
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Siemens" mobile digital X-ray machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f737010898ed2b9909fd878ad5096d0e and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP;; SIEMENS, S.A.. The authorized representative in Taiwan is SIEMENS LIMITED.
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