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"Fotona" Gynecologic general manual instrument (Non-sterile) - Taiwan Registration 4175d4fd1ddd9f06e3d8254125d6fc59

Access comprehensive regulatory information for "Fotona" Gynecologic general manual instrument (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4175d4fd1ddd9f06e3d8254125d6fc59 and manufactured by FOTONA D.O.O.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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4175d4fd1ddd9f06e3d8254125d6fc59
Registration Details
Taiwan FDA Registration: 4175d4fd1ddd9f06e3d8254125d6fc59
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Device Details

"Fotona" Gynecologic general manual instrument (Non-sterile)
TW: "ๅฏŒๅคšๆ‹ฟ"ๅฉฆ็ง‘็”จไธ€่ˆฌๆ‰‹ๅ‹•ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4175d4fd1ddd9f06e3d8254125d6fc59

Ministry of Health Medical Device Import No. 017402

DHA09401740208

Company Information

Slovenia

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".

l Devices for obstetrics and gynecology

L4520 General manual instruments for obstetrics and gynecology

Imported from abroad

Dates and Status

Jan 11, 2017

Jan 11, 2022