Taiwan FDA registration f136120d40b0c4bc10acc2ec0f6b48a4
"Kejie" dental intraosseous implant attachment (unsterilized)
TW: “可捷” 牙齒骨內植入物附件（未滅菌）
Taiwan·Risk Class 1·KJ MEDITECH Co.,Ltd·Registered Jun 22, 2009 – Jun 22, 2014CancelledRegistration details
- Analysis ID
- f136120d40b0c4bc10acc2ec0f6b48a4
- Customs Code
- DHA04400784504
Company information
- Manufacturer
- KJ MEDITECH Co.,Ltd
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Raininbyer GmbH
Product details
- Intended Use
- Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- import
Dates and status
- Registration Date
- Jun 22, 2009
- Expiry Date
- Jun 22, 2014
- 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 "Kejie" dental intraosseous implant 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 f136120d40b0c4bc10acc2ec0f6b48a4 and manufactured by KJ MEDITECH Co.,Ltd. The authorized representative in Taiwan is Raininbyer GmbH.
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