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"Wacoal" in vitro prosthesis (unsterilized) - Taiwan Registration 04172491834a5a05c86041f38b921bfd

Access comprehensive regulatory information for "Wacoal" in vitro prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04172491834a5a05c86041f38b921bfd and manufactured by WACOAL CORP.. The authorized representative in Taiwan is TAIWAN WACOAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TRULIFE, and 2 recent registrations in the same category. 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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04172491834a5a05c86041f38b921bfd
Registration Details
Taiwan FDA Registration: 04172491834a5a05c86041f38b921bfd
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Device Details

"Wacoal" in vitro prosthesis (unsterilized)
TW: โ€œ่ฏๆญŒ็ˆพโ€้ซ”ๅค–็”จ็พฉไนณ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

04172491834a5a05c86041f38b921bfd

DHA04401241805

Company Information

Japan

Product Details

Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).

I General, Plastic Surgery and Dermatology

I.3800 Repair supplement for cosmetic use in the body

import

Dates and Status

Nov 27, 2012

Nov 27, 2022

Sep 30, 2021

Cancellation Information

Logged out

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