"Ayindi" mobile X-ray system
Taiwan·Risk Class 2·INTERMEDICAL S.R.L.·Registered Oct 24, 2011 – Oct 24, 2016Cancelled- Analysis ID
- b2045cc00f3984e7d2c35cb0697c8049
- Customs Code
- DHAS0602290204
- Manufacturer
- INTERMEDICAL S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- FONN CHANG TRADING CO., 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.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
- Registration Date
- Oct 24, 2011
- Expiry Date
- Oct 24, 2016
- Cancellation Date
- Aug 21, 2018
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Ayindi" 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 b2045cc00f3984e7d2c35cb0697c8049 and manufactured by INTERMEDICAL S.R.L.. The authorized representative in Taiwan is FONN CHANG TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including I.M.D. INTERNATIONAL MEDICAL DEVICES S.P.A., and 1 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.