Taiwan FDA registration 1969f6659a457458d953d6434c821aea
Camex Laser Patient Locator (Unsterilized)
TW: “佳美斯”雷射病患定位指示器 (未滅菌)
Taiwan·Risk Class 1·RMI RANGES·Registered Jan 25, 2007 – Jan 25, 2017CancelledRegistration details
- Analysis ID
- 1969f6659a457458d953d6434c821aea
- Customs Code
- DHA04400555307
Company information
- Manufacturer
- RMI RANGES
- Manufacturer Country
- United States
- Authorized Representative
- Qiatai Enterprise Co., Ltd
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Equipment "Patient Positioning Beam Indicator (P.5780)".
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.5780 Patient Positioning Beam Indicator
- Import Information
- import
Dates and status
- Registration Date
- Jan 25, 2007
- Expiry Date
- Jan 25, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Camex Laser Patient Locator (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1969f6659a457458d953d6434c821aea and manufactured by RMI RANGES. The authorized representative in Taiwan is Qiatai Enterprise Co., Ltd.
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