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"Becoen" in vitro cosmetic repair supplement (unsterilized) - Taiwan Registration 467ba8dfbf85210f32c59422cd4247a6

Access comprehensive regulatory information for "Becoen" in vitro cosmetic repair supplement (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 467ba8dfbf85210f32c59422cd4247a6 and manufactured by BECON MEDICAL LIMITED. The authorized representative in Taiwan is Northwest 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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467ba8dfbf85210f32c59422cd4247a6
Registration Details
Taiwan FDA Registration: 467ba8dfbf85210f32c59422cd4247a6
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Device Details

"Becoen" in vitro cosmetic repair supplement (unsterilized)
TW: โ€œๅฟ…่‚ฏโ€้ซ”ๅค–็พŽๅฎน็”จไฟฎๅพฉๅฝŒ่ฃœ็‰ฉ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

467ba8dfbf85210f32c59422cd4247a6

DHA04401034902

Company Information

United States

Product Details

Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).

I General, Plastic Surgery and Dermatology

I.3800 Repair supplement for cosmetic use in the body

import

Dates and Status

May 12, 2011

May 12, 2016

Jun 28, 2018

Cancellation Information

Logged out

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