Taiwan FDA registration aabcce83cc8c6a68b1186144a664cfcd
"Jimmy" Abdominal Inflator Attachment (Unsterilized)
TW: "吉米" 腹腔充氣機附件 (未滅菌)
Taiwan·Risk Class 1·GIMMI GMBH·Registered May 25, 2012 – May 25, 2022CancelledRegistration details
- Analysis ID
- aabcce83cc8c6a68b1186144a664cfcd
- Customs Code
- DHA04401174900
Company information
- Manufacturer
- GIMMI GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BEAMED INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of laparoscopic perfusion device (L.1730) for the management of medical devices.
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1730 腹腔鏡灌入器
- Import Information
- import
Dates and status
- Registration Date
- May 25, 2012
- Expiry Date
- May 25, 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" Abdominal Inflator Attachment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aabcce83cc8c6a68b1186144a664cfcd and manufactured by GIMMI GMBH. The authorized representative in Taiwan is BEAMED INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices