Taiwan FDA registration 6abbbfdba3e5903a050d9bd2744951c3
"Rester" surgical headlamp and its accessories (unsterilized)
TW: "瑞斯特"手術用頭燈及其附件(未滅菌)
Taiwan·Risk Class 1·RUDOLF RIESTER GMBH·Registered Mar 21, 2012 – Mar 21, 2017CancelledRegistration details
- Analysis ID
- 6abbbfdba3e5903a050d9bd2744951c3
- Customs Code
- DHA04401151205
Company information
- Manufacturer
- RUDOLF RIESTER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- XIN BO ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Surgical Headlamps (M.4335)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4335 Headlamps for surgery
- Import Information
- import
Dates and status
- Registration Date
- Mar 21, 2012
- Expiry Date
- Mar 21, 2017
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rester" surgical headlamp and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6abbbfdba3e5903a050d9bd2744951c3 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is XIN BO ENTERPRISE CO., LTD..
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