Taiwan FDA registration 08d522909adeeb188ea352430545ebae
"CILITA" Manual ophthalmic surgical instrument (non-sterile)
TW: "視立達" 手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·CILITA, LLC·Registered Aug 28, 2014 – Aug 28, 2024ExpiredRegistration details
- Analysis ID
- 08d522909adeeb188ea352430545ebae
- License Form
- Ministry of Health Medical Device Import No. 014459
- Customs Code
- DHA09401445909
Company information
- Manufacturer
- CILITA, LLC
- Manufacturer Country
- Russian Federation
- 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
- Aug 28, 2014
- Expiry Date
- Aug 28, 2024
About this record
Access comprehensive regulatory information for "CILITA" 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 08d522909adeeb188ea352430545ebae and manufactured by CILITA, LLC. The authorized representative in Taiwan is AMAZMED CO., LTD..
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