Taiwan FDA registration 6197e7c3cec714043fc85d5647568168
"Rester" rigid laryngoscope (unsterilized)
TW: “瑞斯特”硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·RUDOLF RIESTER GMBH & CO. KG·Registered Jul 04, 2008 – Jul 04, 2013CancelledRegistration details
- Analysis ID
- 6197e7c3cec714043fc85d5647568168
- Customs Code
- DHA04400686709
Company information
- Manufacturer
- RUDOLF RIESTER GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- XIN BO ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- import
Dates and status
- Registration Date
- Jul 04, 2008
- Expiry Date
- Jul 04, 2013
- Cancellation Date
- May 28, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rester" rigid laryngoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6197e7c3cec714043fc85d5647568168 and manufactured by RUDOLF RIESTER GMBH & CO. KG. The authorized representative in Taiwan is XIN BO ENTERPRISE CO., LTD..
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