Taiwan FDA registration 87311b2ce53e6c0c2a3a21829f92d4f2
"OASIS" Manual Ophthalmic Surgical Instrument (Sterile)
TW: "綠洲"手動式眼科手術器械(滅菌)
Taiwan·Risk Class 1·MD·OASIS MEDICAL, INC.·Registered Dec 29, 2017 – Dec 29, 2022ExpiredRegistration details
- Analysis ID
- 87311b2ce53e6c0c2a3a21829f92d4f2
- License Form
- Ministry of Health Medical Device Import No. 018670
- Customs Code
- DHA09401867002
Company information
- Manufacturer
- OASIS MEDICAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- AMAZMED CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4350 Manual Ophthalmic Surgery Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 29, 2017
- Expiry Date
- Dec 29, 2022
About this record
Access comprehensive regulatory information for "OASIS" Manual Ophthalmic Surgical Instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87311b2ce53e6c0c2a3a21829f92d4f2 and manufactured by OASIS MEDICAL, INC.. The authorized representative in Taiwan is AMAZMED CO., LTD..
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