Taiwan FDA registration ca8a8c8d22e0cdea36355c6026c8af9b

"THUASNE" External aesthetic restoration prosthesis (Non-Sterile)

TW: "蘇雅森" 體外美容用修復彌補物 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·THUASNE DEUTSCHLAND GMBH·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
ca8a8c8d22e0cdea36355c6026c8af9b
License Form
Ministry of Health Medical Device Import Registration No. 015990
Customs Code
DHA08401599006
Company information
Manufacturer Country
Germany
Authorized Representative
LUSH INDUSTRIAL CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I3800 In vitro cosmetic repair supplement
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for "THUASNE" External aesthetic restoration prosthesis (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca8a8c8d22e0cdea36355c6026c8af9b and manufactured by THUASNE DEUTSCHLAND GMBH. The authorized representative in Taiwan is LUSH INDUSTRIAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including THUASNE DEUTSCHLAND GMBH, 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.

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