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"Guinici" Demei Gene dermabrasion machine (unsterilized) - Taiwan Registration 00d1dc247c803b3c381c00b529f809d8

Access comprehensive regulatory information for "Guinici" Demei Gene dermabrasion machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 00d1dc247c803b3c381c00b529f809d8 and manufactured by GENESIS BIOSYSTEMS, INC.. The authorized representative in Taiwan is Wo Medical Limited.

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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00d1dc247c803b3c381c00b529f809d8
Registration Details
Taiwan FDA Registration: 00d1dc247c803b3c381c00b529f809d8
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Device Details

"Guinici" Demei Gene dermabrasion machine (unsterilized)
TW: โ€œ็ด€ๅฆฎๅธŒโ€ ๅพท็พŽๅŸบๅ›  ็ฃจ็šฎๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

00d1dc247c803b3c381c00b529f809d8

DHA04401263806

Company Information

United States

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".

I General, Plastic Surgery and Dermatology

I.4820 Surgical Appliances and Accessories or Accessories

import

Dates and Status

Jan 24, 2013

Jan 24, 2018

Dec 13, 2019

Cancellation Information

Logged out

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