Taiwan FDA registration 64dfc1bb9703545876b156343642f175
"Kelster" ENT manual surgical instruments (unsterilized)
TW: "凱爾史特"耳鼻喉手動式外科器械(未滅菌)
Taiwan·Risk Class 1·KARL STORZ GMBH&CO. KG·Registered May 13, 2011 – May 13, 2016CancelledRegistration details
- Analysis ID
- 64dfc1bb9703545876b156343642f175
- Customs Code
- DHA04401036105
Company information
- Manufacturer
- KARL STORZ GMBH&CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- Jiatai Medical Equipment 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
- May 13, 2011
- Expiry Date
- May 13, 2016
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kelster" 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 64dfc1bb9703545876b156343642f175 and manufactured by KARL STORZ GMBH&CO. KG. The authorized representative in Taiwan is Jiatai Medical Equipment Co., Ltd.
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