Taiwan FDA registration da21ec150e53d8da417eaa5ba4696f4c
"Gyrus" Ear, nose, and throat examination and treatment unit (Non-Sterile)
TW: "吉洛氏" 耳鼻喉檢查及治療檯 (未滅菌)
Taiwan·Risk Class 1·MD·GYRUS MEDICAL GMBH·Registered Sep 06, 2013 – Sep 06, 2018CancelledRegistration details
- Analysis ID
- da21ec150e53d8da417eaa5ba4696f4c
- License Form
- Ministry of Health Medical Device Import No. 013391
- Customs Code
- DHA09401339109
Company information
- Manufacturer
- GYRUS MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Yuanyou Industrial Co., Ltd
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G5300 ENT Examination and Treatment Unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 06, 2013
- Expiry Date
- Sep 06, 2018
- 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 "Gyrus" Ear, nose, and throat examination and treatment unit (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 da21ec150e53d8da417eaa5ba4696f4c and manufactured by GYRUS MEDICAL GMBH. The authorized representative in Taiwan is Yuanyou Industrial Co., Ltd.
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