Taiwan FDA registration ead726b8a5aa1978b935465da4f0a235
"Singular" mobile X-ray system
TW: "奇異" 移動式X光系統
Taiwan·Risk Class 2·GE MEDICAL SYSTEMS, LLC·Registered Feb 01, 2005 – Feb 01, 2030ActiveRegistration details
- Analysis ID
- ead726b8a5aa1978b935465da4f0a235
- Customs Code
- DHAS0601103600
Company information
- Manufacturer
- GE MEDICAL SYSTEMS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
- Intended Use
- AMX-4+, blank below.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1720 移動式X光系統
- 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
- Feb 01, 2005
- Expiry Date
- Feb 01, 2030
About this record
Access comprehensive regulatory information for "Singular" mobile 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 ead726b8a5aa1978b935465da4f0a235 and manufactured by GE MEDICAL SYSTEMS, LLC. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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