"Arkema" X-ray diagnostic system - Taiwan Registration 704f4fa7b9e70695eb39638a4eab3c32
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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
P Radiology Science
P.1680 ๅบๅฎๅผXๅ ็ณป็ตฑ
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and Status
Sep 27, 2017
Sep 27, 2027