Taiwan FDA registration c15a9dd655ec5434d6e7877ee6ff3d92
"Riester" Rigid laryngoscope (Non-Sterile)
TW: "瑞司" 硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·MD·Rudolf Riester GmbH·Registered May 19, 2017 – May 19, 2027ActiveRegistration details
- Analysis ID
- c15a9dd655ec5434d6e7877ee6ff3d92
- License Form
- Ministry of Health Medical Device Import No. 017859
- Customs Code
- DHA09401785901
Company information
- Manufacturer
- Rudolf Riester GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BOYANG MEDICAL TECHNOLOGY 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 Devices for anesthesiology
- Product Type (Level 2)
- D5540 Rigid laryngoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 19, 2017
- Expiry Date
- May 19, 2027
About this record
Access comprehensive regulatory information for "Riester" Rigid laryngoscope (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 c15a9dd655ec5434d6e7877ee6ff3d92 and manufactured by Rudolf Riester GmbH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.
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