Taiwan FDA registration 4b31209fa85289f2e60601b64ceba290
"RET" Manual Ophthalmic Surgical Instrument (non-sterile)
TW: "瑞英特"手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·MD·RET, INC.·Registered Mar 18, 2019 – Mar 18, 2024ExpiredRegistration details
- Analysis ID
- 4b31209fa85289f2e60601b64ceba290
- License Form
- Ministry of Health Medical Device Import No. 020198
- Customs Code
- DHA09402019806
Company information
- Manufacturer
- RET, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CONEYE 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
- Mar 18, 2019
- Expiry Date
- Mar 18, 2024
About this record
Access comprehensive regulatory information for "RET" Manual Ophthalmic Surgical 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 4b31209fa85289f2e60601b64ceba290 and manufactured by RET, INC.. The authorized representative in Taiwan is CONEYE CO., LTD.
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