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Primsulis non-invasive treatment device - Taiwan Registration a347aec9bb39ff20031ba96e8902053a

Access comprehensive regulatory information for Primsulis non-invasive treatment device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a347aec9bb39ff20031ba96e8902053a and manufactured by DAEYANG MEDICAL Co., Ltd. The authorized representative in Taiwan is CLOVERS 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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a347aec9bb39ff20031ba96e8902053a
Registration Details
Taiwan FDA Registration: a347aec9bb39ff20031ba96e8902053a
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Device Details

Primsulis non-invasive treatment device
TW: ๅ…ˆ่ˆ’็ซ‹้žไพตๅ…ฅๅผๆฒป็™‚่ฃ็ฝฎ
Risk Class 2

Registration Details

a347aec9bb39ff20031ba96e8902053a

DHA05603486805

Company Information

Korea, Republic of

Product Details

It is used for pelvic floor muscle strengthening in the treatment of urinary incontinence.

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H.5320 Non-implantable electronic urination home-made device;; O.5850 Powered Muscle Stimulator

import

Dates and Status

Oct 04, 2021

Oct 04, 2026