Taiwan FDA registration dfb8ed160c4d92ee0975c1edd2810581
"Thunderbolt" patient positioning beam indicator (not sterilized)
TW: “雷波雷射”病患定位光束指示器 (未滅菌)
Taiwan·Risk Class 1·LAPLASER APPLIKATIONEN GMBH·Registered Aug 31, 2006 – Aug 31, 2011CancelledRegistration details
- Analysis ID
- dfb8ed160c4d92ee0975c1edd2810581
- Customs Code
- DHA04400510608
Company information
- Manufacturer
- LAPLASER APPLIKATIONEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Exuberant International Enterprises Limited
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
- Aug 31, 2006
- Expiry Date
- Aug 31, 2011
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Thunderbolt" patient positioning beam indicator (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfb8ed160c4d92ee0975c1edd2810581 and manufactured by LAPLASER APPLIKATIONEN GMBH. The authorized representative in Taiwan is Exuberant International Enterprises Limited.
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