"Arkema" X-ray diagnostic system
Taiwan·Risk Class 2·Arcoma AB·Registered Jan 25, 2018 – Jan 25, 2028Active- Analysis ID
- b9404d295750282b63f8d0c27b8dd7db
- Customs Code
- DHAS5603071507
- Manufacturer
- Arcoma AB
- Manufacturer Country
- Sweden
- Authorized Representative
- NAN KAI CORPORATION
- 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.1680 固定式X光系統
- 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
- Jan 25, 2018
- Expiry Date
- Jan 25, 2028
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Access comprehensive regulatory information for "Arkema" X-ray diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b9404d295750282b63f8d0c27b8dd7db and manufactured by Arcoma AB. The authorized representative in Taiwan is NAN KAI CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Arcoma AB, 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.