"Singular" fluoroscopic X-ray system
Taiwan·Risk Class 2·GE MEDICAL SYSTEMS S.A.·Registered Oct 04, 2005 – Oct 04, 2015Cancelled- Analysis ID
- 68af0d634fd08ade0e04080894fd77ed
- Customs Code
- DHAS0601260202
- Manufacturer
- GE MEDICAL SYSTEMS S.A.
- Manufacturer Country
- France
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- 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.1650 透視X光影像增感管
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
- Registration Date
- Oct 04, 2005
- Expiry Date
- Oct 04, 2015
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Singular" fluoroscopic 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 68af0d634fd08ade0e04080894fd77ed and manufactured by GE MEDICAL SYSTEMS S.A.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including GENERAL MEDICAL MERATE S.P.A., GE MEDICAL SYSTEMS S.A., and 5 recent registrations in the same category. 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.