Taiwan FDA registration 47da1063c2c763e2049d75758aa81d62
"Solokmai" ENT light source and its accessories (unsterilized)
TW: “所波羅克邁”耳鼻喉科用光源及其附件(未滅菌)
Taiwan·Risk Class 1·BLOW-COMEG·Registered Nov 30, 2007 – Nov 30, 2022CancelledRegistration details
- Analysis ID
- 47da1063c2c763e2049d75758aa81d62
- Customs Code
- DHA04400633900
Company information
- Manufacturer
- BLOW-COMEG
- Manufacturer Country
- France
- Authorized Representative
- Chengyi Limited
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4350 Ear, nose and throat optical fiber light sources and carriers
- Import Information
- import
Dates and status
- Registration Date
- Nov 30, 2007
- Expiry Date
- Nov 30, 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 "Solokmai" ENT light source and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 47da1063c2c763e2049d75758aa81d62 and manufactured by BLOW-COMEG. The authorized representative in Taiwan is Chengyi Limited.
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