Taiwan FDA registration e338ec2426458a1dd2c1c85e59883fb9
"Ophtec" Manual Ophthalmic Surgical Instrument (Non-Sterile)
TW: "歐斯提克"手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·OPHTEC B.V.·Registered Feb 27, 2014 – Feb 27, 2019CancelledRegistration details
- Analysis ID
- e338ec2426458a1dd2c1c85e59883fb9
- License Form
- Ministry of Health Medical Device Import No. 013897
- Customs Code
- DHA09401389702
Company information
- Manufacturer
- OPHTEC B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- 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
- Feb 27, 2014
- Expiry Date
- Feb 27, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ophtec" 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 e338ec2426458a1dd2c1c85e59883fb9 and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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