Taiwan FDA registration c795d2f4b4787a8abea7192bd8826bb9
"Jimmy" endoscopes and instruments and accessories for endoscopic surgery
TW: "吉米"內視鏡及內視鏡手術用器械及附件
Taiwan·Risk Class 2·GIMMI GMBH.·Registered Jun 19, 2006 – Jun 19, 2021CancelledRegistration details
- Analysis ID
- c795d2f4b4787a8abea7192bd8826bb9
- Customs Code
- DHA00601670508
Company information
- Manufacturer
- GIMMI GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- BEAMED INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Jun 19, 2006
- Expiry Date
- Jun 19, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jimmy" endoscopes and instruments and accessories for endoscopic surgery in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c795d2f4b4787a8abea7192bd8826bb9 and manufactured by GIMMI GMBH.. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
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