Taiwan FDA registration f1f74c1087eee04ade17226fdf89dc60
"Schweimer" two-way G-arm X-ray machine
TW: “史威邁”雙向G臂X光機
Taiwan·Risk Class 2·SWEMAC MEDICAL APPLIANCES AB·Registered May 07, 2019 – May 07, 2029ActiveRegistration details
- Analysis ID
- f1f74c1087eee04ade17226fdf89dc60
- Customs Code
- DHAS5603259800
Company information
- Manufacturer
- SWEMAC MEDICAL APPLIANCES AB
- Manufacturer Country
- Sweden
- Authorized Representative
- GREENEVER MEDICAL SYSTEMS INC .
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- May 07, 2019
- Expiry Date
- May 07, 2029
About this record
Access comprehensive regulatory information for "Schweimer" two-way G-arm 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 f1f74c1087eee04ade17226fdf89dc60 and manufactured by SWEMAC MEDICAL APPLIANCES AB. The authorized representative in Taiwan is GREENEVER MEDICAL SYSTEMS INC ..
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