"Arkema" X-ray diagnostic system
Taiwan·Risk Class 2·Arcoma AB·Registered Sep 27, 2017 – Sep 27, 2027Active- Analysis ID
- 704f4fa7b9e70695eb39638a4eab3c32
- Customs Code
- DHAS5603026107
- 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
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
- Registration Date
- Sep 27, 2017
- Expiry Date
- Sep 27, 2027
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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 704f4fa7b9e70695eb39638a4eab3c32 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.