Taiwan FDA registration 6c7c6cc0d460dcfc1ee9bfec2b51a3d5
“Aesculap”Rigid laryngoscope (Non-sterile)
TW: “雅氏”硬式喉頭鏡 (未滅菌)
Taiwan·Risk Class 1·MD·AESCULAP AG·Registered Jul 01, 2020 – Jul 01, 2025ExpiredRegistration details
- Analysis ID
- 6c7c6cc0d460dcfc1ee9bfec2b51a3d5
- License Form
- Ministry of Health Medical Device Import No. 021684
- Customs Code
- DHA09402168407
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN 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
- Jul 01, 2020
- Expiry Date
- Jul 01, 2025
About this record
Access comprehensive regulatory information for “Aesculap”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 6c7c6cc0d460dcfc1ee9bfec2b51a3d5 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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