"Arthroscopy" arthroscopy and its accessories - Taiwan Registration 283621279eab13cde3a6f9f638d2cd6f
Access comprehensive regulatory information for "Arthroscopy" arthroscopy and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 283621279eab13cde3a6f9f638d2cd6f and manufactured by AESCULAP AG. The authorized representative in Taiwan is Taiwan Birlanc Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. 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.
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283621279eab13cde3a6f9f638d2cd6f
Registration Details
Taiwan FDA Registration: 283621279eab13cde3a6f9f638d2cd6f
Device Details
"Arthroscopy" arthroscopy and its accessories
TW: "้
ๆฐ" ้็ฏ้กๅๅ
ถ้ไปถ
Risk Class 2
Cancelled

