"Arkema" X-ray diagnostic system - Taiwan Registration b9404d295750282b63f8d0c27b8dd7db
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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
P Radiology Science
P.1680 ๅบๅฎๅผXๅ ็ณป็ตฑ
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and Status
Jan 25, 2018
Jan 25, 2028