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"Doctor Derma" silicone gel (Non-sterile) - Taiwan Registration 08f08f38113703d053a7022552154e92

Access comprehensive regulatory information for "Doctor Derma" silicone gel (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 08f08f38113703d053a7022552154e92 and manufactured by SUNGJI MEDICAL CO.. The authorized representative in Taiwan is HORIZON INSTRUMENTS 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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08f08f38113703d053a7022552154e92
Registration Details
Taiwan FDA Registration: 08f08f38113703d053a7022552154e92
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Device Details

"Doctor Derma" silicone gel (Non-sterile)
TW: "้Ÿ“ๅพ—็พŽ" ็–ค็—•่ญท็†ๅ‡่†  (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

08f08f38113703d053a7022552154e92

Ministry of Health Medical Device Import No. 017441

DHA09401744105

Company Information

Korea, Republic of

Product Details

Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".

I General and plastic surgical devices

I4025 Scar Treatment Silicone Products

Imported from abroad

Dates and Status

Jan 19, 2017

Jan 19, 2027