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"Hanshi" Mitrati line - Taiwan Registration 2b2a81d69d5451d8ca814492d3f66e50

Access comprehensive regulatory information for "Hanshi" Mitrati line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b2a81d69d5451d8ca814492d3f66e50 and manufactured by HansBiomed Corp.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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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2b2a81d69d5451d8ca814492d3f66e50
Registration Details
Taiwan FDA Registration: 2b2a81d69d5451d8ca814492d3f66e50
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Device Details

"Hanshi" Mitrati line
TW: โ€œ้Ÿ“ๅฃซโ€็ง˜็‰นๆ‹‰ๆ็ทš
Risk Class 2

Registration Details

2b2a81d69d5451d8ca814492d3f66e50

DHA05603478208

Company Information

Korea, Republic of

Product Details

This product is suitable for mid-face lift surgery and temporarily fixes the subcutaneous fat layer and superficial muscle membrane system layer (SMAS layer) of the cheek in a higher position for the treatment of mild to moderate nasolabial folds.

I General, Plastic Surgery and Dermatology

I.4840 Absorbable polydioxanone surgical joint

Safety monitoring;; import

Dates and Status

Sep 08, 2021

Sep 08, 2026