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"Yobamei" Skin Irritation Bottle (Sterilized) - Taiwan Registration 2422726aef073d34271099782a725ac2

Access comprehensive regulatory information for "Yobamei" Skin Irritation Bottle (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2422726aef073d34271099782a725ac2 and manufactured by U-BIOMED INC.. The authorized representative in Taiwan is HAO SHAN BIOTECHNOLOGY 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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2422726aef073d34271099782a725ac2
Registration Details
Taiwan FDA Registration: 2422726aef073d34271099782a725ac2
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Device Details

"Yobamei" Skin Irritation Bottle (Sterilized)
TW: "ๅ„ช็™พๅชš" ็šฎ่†šๅˆบๆฟ€็“ถ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2422726aef073d34271099782a725ac2

DHA09401601904

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Input;; QMS/QSD

Dates and Status

Dec 28, 2015

Dec 28, 2020

Jul 15, 2022

Cancellation Information

Logged out

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