Taiwan FDA registration 1a1210c41f55b144e594eb7d81669eb2
"Ripreel" beam patient positioning indicator (unsterilized)
TW: “雷普雷射”光束病患定位指示燈 （未滅菌）
Taiwan·Risk Class 1·LAPLASER APPLIKATIONEN GMBH·Registered Nov 02, 2006 – Nov 02, 2016CancelledRegistration details
- Analysis ID
- 1a1210c41f55b144e594eb7d81669eb2
- Customs Code
- DHA04400529702
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 Radiology Science
- Product Type (Level 2)
- P.5780 Patient Positioning Beam Indicator
- Import Information
- import
Dates and status
- Registration Date
- Nov 02, 2006
- Expiry Date
- Nov 02, 2016
- Cancellation Date
- Nov 18, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for "Ripreel" beam patient positioning indicator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1a1210c41f55b144e594eb7d81669eb2 and manufactured by LAPLASER APPLIKATIONEN GMBH. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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