Taiwan FDA registration a9f2b439d581003d2bfeb62097e30d76

"Mortan" Ocular Surgery Irrigation Device (Non-Sterile)

TW: "摩頓" 眼科手術灌注裝置 (未滅菌)

Taiwan·Risk Class 1·MD·MORTAN, INC.·Registered Nov 25, 2016 – Nov 25, 2021Expired

Registration details

Analysis ID: a9f2b439d581003d2bfeb62097e30d76
License Form: Ministry of Health Medical Device Import No. 017211
Customs Code: DHA09401721101

Company information

Manufacturer: MORTAN, INC.
Manufacturer Country: United States
Authorized Representative: BIOMEGA INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Eye Surgical Perfusion Device (M.4360)".
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M4360 Surgical perfusion device for the eye
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 25, 2016
Expiry Date: Nov 25, 2021

About this record

Access comprehensive regulatory information for "Mortan" Ocular Surgery Irrigation Device (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 a9f2b439d581003d2bfeb62097e30d76 and manufactured by MORTAN, INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..

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