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FACILLE Rouge Light Facial Dermal Implant - Taiwan Registration 89920a691efab891dec2e9e3e6c1b20e

Access comprehensive regulatory information for FACILLE Rouge Light Facial Dermal Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 89920a691efab891dec2e9e3e6c1b20e and manufactured by SCIVISION BIOTECH INC.. The authorized representative in Taiwan is SCIVISION BIOTECH INC..

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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89920a691efab891dec2e9e3e6c1b20e
Registration Details
Taiwan FDA Registration: 89920a691efab891dec2e9e3e6c1b20e
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Device Details

FACILLE Rouge Light Facial Dermal Implant
TW: ๆณ•ๆ€้บ—ๆŸ”ๅงฟ่ผ•ๆ„Ÿ็šฎไธ‹ๅกซ่ฃœๅŠ‘
Risk Class 3
MD

Registration Details

89920a691efab891dec2e9e3e6c1b20e

Ministry of Health Medical Device Manufacturing No. 006939

Company Information

Taiwan, Province of China

Product Details

Limited to the scope of identification of "hyaluronic acid implants (I.0007)" of the Measures for the Administration of Medical Devices.

I General and plastic surgical devices

I0007 Hyaluronic acid implants

Produced in Taiwan, China

Dates and Status

Dec 03, 2020

Mar 01, 2026