Taiwan FDA registration b8cd9acbda30dfc7565216293edc1faa
"Jimmy" ENT fiber optic light source and vehicle (unsterilized)
TW: “吉米”耳鼻喉光纖光源及載具(未滅菌)
Taiwan·Risk Class 1·GIMMI GMBH·Registered May 18, 2012 – May 18, 2022CancelledRegistration details
- Analysis ID
- b8cd9acbda30dfc7565216293edc1faa
- Customs Code
- DHA04401172305
Company information
- Manufacturer
- GIMMI GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BEAMED INSTRUMENTS CO., LTD.
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
- May 18, 2012
- Expiry Date
- May 18, 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 "Jimmy" ENT fiber optic light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b8cd9acbda30dfc7565216293edc1faa and manufactured by GIMMI GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
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