Taiwan FDA registration fcbccb50593afac0303f8343420d5366
"Ambo" otoscopy (unsterilized)
TW: “安伏”耳鏡 (未滅菌)
Taiwan·Risk Class 1·RF CO., LTD.·Registered Sep 20, 2006 – Sep 20, 2011CancelledRegistration details
- Analysis ID
- fcbccb50593afac0303f8343420d5366
- Customs Code
- DHA04400517909
Company information
- Manufacturer
- RF CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Zongteng Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4770 Ear Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Sep 20, 2006
- Expiry Date
- Sep 20, 2011
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ambo" otoscopy (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fcbccb50593afac0303f8343420d5366 and manufactured by RF CO., LTD.. The authorized representative in Taiwan is Zongteng Technology Co., Ltd.
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