Taiwan FDA registration ed04045778b815aebefc21d2429d5de7
"SOPRO-COMEG" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "舒博-柯曼" 耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·MD·SOPRO-COMEG GMBH·Registered Jan 13, 2015 – Jan 13, 2020CancelledRegistration details
- Analysis ID
- ed04045778b815aebefc21d2429d5de7
- License Form
- Ministry of Health Medical Device Import No. 014840
- Customs Code
- DHA09401484004
Company information
- Manufacturer
- SOPRO-COMEG GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- FU TAI TRADING CO., LTD.
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 13, 2015
- Expiry Date
- Jan 13, 2020
- 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 "SOPRO-COMEG" Ear, nose, and throat fiberoptic light source and carrier (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 ed04045778b815aebefc21d2429d5de7 and manufactured by SOPRO-COMEG GMBH. The authorized representative in Taiwan is FU TAI TRADING CO., LTD..
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