Taiwan FDA registration 4175d4fd1ddd9f06e3d8254125d6fc59

"Fotona" Gynecologic general manual instrument (Non-sterile)

TW: "富多拿"婦科用一般手動器械 (未滅菌)

Taiwan·Risk Class 1·MD·FOTONA D.O.O.·Registered Jan 11, 2017 – Jan 11, 2022Expired

Registration details

Analysis ID: 4175d4fd1ddd9f06e3d8254125d6fc59
License Form: Ministry of Health Medical Device Import No. 017402
Customs Code: DHA09401740208

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: Jan 11, 2017
Expiry Date: Jan 11, 2022

About this record

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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