Taiwan FDA registration f22fc082bf5f06f660e773e5133552e0
"Ekler" Ilio dental surgical light (unsterilized)
TW: "艾克樂" 伊利歐牙科用手術燈 (未滅菌)
Taiwan·Risk Class 1·ECLAIR·Registered Jul 17, 2017 – Jul 17, 2022CancelledRegistration details
- Analysis ID
- f22fc082bf5f06f660e773e5133552e0
- Customs Code
- DHA09401807103
Company information
- Manufacturer
- ECLAIR
- Manufacturer Country
- France
- Authorized Representative
- QUEN LIN INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Dental Surgical Light (F.4630)" and "Dental Surgical Devices and Their Accessories (F.6640)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.6640 牙科手術裝置及其附件;; F.4630 牙科用手術燈
- Import Information
- import
Dates and status
- Registration Date
- Jul 17, 2017
- Expiry Date
- Jul 17, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ekler" Ilio dental surgical light (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f22fc082bf5f06f660e773e5133552e0 and manufactured by ECLAIR. The authorized representative in Taiwan is QUEN LIN INSTRUMENTS CO., LTD..
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