Taiwan FDA registration f4af7abf45dc58ad279ad272059cdb40
"Siemens" mobile X-ray machine for whole body diagnostics
TW: "西門子" 全身診斷用移動式X光機
Taiwan·Risk Class 2·SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP;; SIEMENS, S.A.·Registered Nov 22, 2005 – Nov 22, 2015CancelledRegistration details
- Analysis ID
- f4af7abf45dc58ad279ad272059cdb40
- Customs Code
- DHAS0601362901
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
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Nov 22, 2005
- Expiry Date
- Nov 22, 2015
- 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 X-ray machine for whole body diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4af7abf45dc58ad279ad272059cdb40 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