Taiwan FDA registration e5784a0a6318dd308b61db99f4c521b3
Pengwei Discarded laryngoscope (unsterilized)
TW: 鵬維 拋棄式喉頭鏡(未滅菌)
Taiwan·Risk Class 1·PENG WAVES ENTERPRISE CO., LTD.·Registered Sep 13, 2005 – Sep 13, 2025ExpiredRegistration details
- Analysis ID
- e5784a0a6318dd308b61db99f4c521b3
- Customs Code
- DHY04300017001
Company information
- Manufacturer
- PENG WAVES ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PENG WAVES ENTERPRISE CO., LTD.
Product details
- Intended Use
- It is used to examine and examine the patient's upper airway and assist in the placement of endotracheal intubation.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5540 Rigid laryngoscope
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 13, 2005
- Expiry Date
- Sep 13, 2025
About this record
Access comprehensive regulatory information for Pengwei Discarded 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 e5784a0a6318dd308b61db99f4c521b3 and manufactured by PENG WAVES ENTERPRISE CO., LTD.. The authorized representative in Taiwan is PENG WAVES ENTERPRISE CO., LTD..
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