Taiwan FDA registration d3d1f7a12bdf812b84f0eeabeae8a4c3

"Fotona" Obstetric-gynecologic general manual instrument (Non-sterile)

TW: "富多拿" 婦產科用一般手動器械 (未滅菌)

Taiwan·Risk Class 1·MD·FOTONA D.O.O.·Registered Mar 25, 2015 – Mar 25, 2025Expired

Registration details

Analysis ID: d3d1f7a12bdf812b84f0eeabeae8a4c3
License Form: Ministry of Health Medical Device Import No. 015042
Customs Code: DHA09401504207

Company information

Manufacturer: FOTONA D.O.O.
Manufacturer Country: Slovenia
Authorized Representative: DYNAMIC MEDICAL TECHNOLOGIES INC.

Product details

Intended Use: 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)".
Product Type (Level 1): l Devices for obstetrics and gynecology
Product Type (Level 2): L4520 General manual instruments for obstetrics and gynecology
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 25, 2015
Expiry Date: Mar 25, 2025

About this record

Access comprehensive regulatory information for "Fotona" Obstetric-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 d3d1f7a12bdf812b84f0eeabeae8a4c3 and manufactured by FOTONA D.O.O.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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.