Taiwan FDA registration 34c259cbcc56c659d7c6e34ad190378d
"Siemens" whole body diagnostic X-ray system
TW: "西門子"全身診斷X光系統
Taiwan·Risk Class 2·SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP·Registered Jun 14, 2006 – Jun 14, 2016CancelledRegistration details
- Analysis ID
- 34c259cbcc56c659d7c6e34ad190378d
- Customs Code
- DHAS0601667800
Company information
- Manufacturer
- SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP
- Manufacturer Country
- 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
- Jun 14, 2006
- Expiry Date
- Jun 14, 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" whole body diagnostic X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 34c259cbcc56c659d7c6e34ad190378d 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. 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