Taiwan FDA registration 7dd3429ea7c3ff885df1c8f8fedae7d9
"Rester" manual stethoscope (unsterilized)
TW: "瑞斯特"手動聽診器(未滅菌)
Taiwan·Risk Class 1·RUDOLF RIESTER GMBH·Registered Aug 18, 2011 – Aug 18, 2016CancelledRegistration details
- Analysis ID
- 7dd3429ea7c3ff885df1c8f8fedae7d9
- Customs Code
- DHA04401072606
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 "stethoscope (E.1875)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1875 Listening device
- Import Information
- import
Dates and status
- Registration Date
- Aug 18, 2011
- Expiry Date
- Aug 18, 2016
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rester" manual stethoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7dd3429ea7c3ff885df1c8f8fedae7d9 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is XIN BO ENTERPRISE CO., LTD..
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