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Vibella soft tissue implants - Taiwan Registration 5b982de69629ba11dec4f64f9b323410

Access comprehensive regulatory information for Vibella soft tissue implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5b982de69629ba11dec4f64f9b323410 and manufactured by VAIM Co., Ltd.. The authorized representative in Taiwan is MEGAMEDI International Ent. 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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5b982de69629ba11dec4f64f9b323410
Registration Details
Taiwan FDA Registration: 5b982de69629ba11dec4f64f9b323410
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Device Details

Vibella soft tissue implants
TW: ่–‡่ฒๆ‹‰่ปŸ็ต„็น”ๆคๅ…ฅๅŠ‘
Risk Class 3

Registration Details

5b982de69629ba11dec4f64f9b323410

DHA05603650607

Company Information

Korea, Republic of

Product Details

This product is used to fill the depression in the nasolabial fold intradermally and subcutaneously in adults aged 19 and above to increase the volume of soft tissues and correct tissue asymmetry.

I General, Plastic Surgery and Dermatology

I.9999 Miscellaneous

import

Dates and Status

Oct 16, 2023

Oct 16, 2028