Taiwan FDA registration ff4004b98e9f74ebb0f250202fc6ab65

"Eufoton" Obstetric-gynecologic general manual instrument (Non-Sterile)

TW: "優芙登" 婦產科用一般手動器械 (未滅菌)

Taiwan·Risk Class 1·MD·EUFOTON S.R.L.·Registered Apr 05, 2017 – Apr 05, 2022Expired

Registration details

Analysis ID: ff4004b98e9f74ebb0f250202fc6ab65
License Form: Ministry of Health Medical Device Import No. 017681
Customs Code: DHA09401768102

Company information

Manufacturer: EUFOTON S.R.L.
Manufacturer Country: Italy
Authorized Representative: WAY SEEN INTERNATIONAL CO., LTD.

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: Apr 05, 2017
Expiry Date: Apr 05, 2022

About this record

Access comprehensive regulatory information for "Eufoton" 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 ff4004b98e9f74ebb0f250202fc6ab65 and manufactured by EUFOTON S.R.L.. The authorized representative in Taiwan is WAY SEEN INTERNATIONAL CO., LTD..

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