Taiwan FDA registration 149cb51b352a203d2986109e6dac167b
"Ji Qi" Al Fidalip ENT Manual Surgical Instruments (Unsterilized)
TW: “吉銤”艾爾菲達力普 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·GIMMI GMBH.·Registered Feb 15, 2007 – Feb 15, 2022CancelledRegistration details
- Analysis ID
- 149cb51b352a203d2986109e6dac167b
- Customs Code
- DHA04400561401
Company information
- Manufacturer
- GIMMI GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4420 Otolaryngology manual surgical instruments
- Import Information
- import
Dates and status
- Registration Date
- Feb 15, 2007
- Expiry Date
- Feb 15, 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 "Ji Qi" Al Fidalip ENT Manual Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 149cb51b352a203d2986109e6dac167b and manufactured by GIMMI GMBH.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..
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