Taiwan FDA registration 7038ebf73a3dc349290025acb41f68fa
"Oertli" Manual Ophthalmic Surgical Instrument (Non-Sterile)
TW: "歐特利" 手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·OERTLI INSTRUMENTE AG·Registered Nov 19, 2019 – Nov 19, 2024ExpiredRegistration details
- Analysis ID
- 7038ebf73a3dc349290025acb41f68fa
- License Form
- Ministry of Health Medical Device Import No. 021024
- Customs Code
- DHA09402102404
Company information
- Manufacturer
- OERTLI INSTRUMENTE AG
- Manufacturer Country
- Switzerland
- 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
- Nov 19, 2019
- Expiry Date
- Nov 19, 2024
About this record
Access comprehensive regulatory information for "Oertli" 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 7038ebf73a3dc349290025acb41f68fa and manufactured by OERTLI INSTRUMENTE AG. The authorized representative in Taiwan is CONEYE CO., LTD.
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