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"Day Trip" Cremei artificial leather hydrophilic waterproof tripping patch (sterilized) - Taiwan Registration 48eb7ccfafe4f78420aeabb06255c810

Access comprehensive regulatory information for "Day Trip" Cremei artificial leather hydrophilic waterproof tripping patch (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 48eb7ccfafe4f78420aeabb06255c810 and manufactured by NICHIBAN MEDICAL CORP.. The authorized representative in Taiwan is TAIWAN NIPPON KAYAKU 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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48eb7ccfafe4f78420aeabb06255c810
Registration Details
Taiwan FDA Registration: 48eb7ccfafe4f78420aeabb06255c810
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Device Details

"Day Trip" Cremei artificial leather hydrophilic waterproof tripping patch (sterilized)
TW: โ€œๆ—ฅ็ต†โ€ ๅฏ้บ—็พŽไบบๅทฅ็šฎ่ฆชๆฐดๆ€ง้˜ฒๆฐด็ต†ๅ‰ต่ฒผๅธƒ(ๆป…่Œ)
Risk Class 1

Registration Details

48eb7ccfafe4f78420aeabb06255c810

DHA09401923907

Company Information

Japan

Product Details

Limited to the first level recognition range of the classification and grading management measures for medical equipment "hydrophilic trauma covering materials (I.4018)".

I General, Plastic Surgery and Dermatology

I.4018 ่ฆชๆฐดๆ€งๅ‰ตๅ‚ท่ฆ†่“‹ๆ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jun 27, 2018

Jun 27, 2028