Taiwan FDA registration 856c7b6c95ee2c3e29dc72248c694acb
"LAPLASER" Light Beam Patient Position Indicator (Non-Sterile)
TW: "雷普雷射" 光束病患定位指示燈 (未滅菌)
Taiwan·Risk Class 1·MD·LAPLASER APPLIKATIONEN GMBH·Registered Nov 17, 2016 – Nov 17, 2021ExpiredRegistration details
- Analysis ID
- 856c7b6c95ee2c3e29dc72248c694acb
- License Form
- Ministry of Health Medical Device Import No. 017189
- Customs Code
- DHA09401718908
Company information
- Manufacturer
- LAPLASER APPLIKATIONEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, 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 Devices for radiology
- Product Type (Level 2)
- P5780 Patient Positioning Beam Indicator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 17, 2016
- Expiry Date
- Nov 17, 2021
About this record
Access comprehensive regulatory information for "LAPLASER" Light Beam Patient Position Indicator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 856c7b6c95ee2c3e29dc72248c694acb and manufactured by LAPLASER APPLIKATIONEN GMBH. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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