Taiwan FDA registration 3b84be424b2271f46873576af41f6b22

"Oyasis" manual ophthalmic surgical instruments (sterilization)

TW: "歐雅西斯"手動式眼科手術器械(滅菌)

Taiwan·Risk Class 1·OASIS MEDICAL INC.·Registered Mar 16, 2012 – Mar 16, 2027Active

Registration details

Analysis ID: 3b84be424b2271f46873576af41f6b22
Customs Code: DHA04401148209

Company information

Manufacturer: OASIS MEDICAL INC.
Manufacturer Country: United States
Authorized Representative: RAY HUNG INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.4350 手動式眼科手術器械
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Mar 16, 2012
Expiry Date: Mar 16, 2027

About this record

Access comprehensive regulatory information for "Oyasis" manual ophthalmic surgical instruments (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3b84be424b2271f46873576af41f6b22 and manufactured by OASIS MEDICAL INC.. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..

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