Taiwan FDA registration d19fe1ff5df732650c936e7af71bef53
“GIMMI” Alphaduolap Insufflator
TW: “吉米”阿爾法杜樂普腹腔鏡灌入器
Taiwan·Risk Class 2·MD·GIMMI GMBH·Registered Nov 03, 2015 – Nov 03, 2020CancelledRegistration details
- Analysis ID
- d19fe1ff5df732650c936e7af71bef53
- License Form
- Ministry of Health Medical Device Import No. 027839
- Customs Code
- DHA05602783907
Company information
- Manufacturer
- GIMMI GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BEAMED INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L1730 Laparoscopic perfusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 03, 2015
- Expiry Date
- Nov 03, 2020
- Cancellation Date
- Dec 07, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “GIMMI” Alphaduolap Insufflator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d19fe1ff5df732650c936e7af71bef53 and manufactured by GIMMI GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
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