Taiwan FDA registration 4c46b690f3c238512dc170d3358da8b3
"LifeVac" Tracheobronchial suction catheter (Non-sterile)
TW: "力哈" 手動喉嚨異物抽吸器 (未滅菌)
Taiwan·Risk Class 1·MD·LIFEVAC LLC·Registered Feb 05, 2020 – Feb 05, 2025ExpiredRegistration details
- Analysis ID
- 4c46b690f3c238512dc170d3358da8b3
- License Form
- Ministry of Health Medical Device Import No. 021226
- Customs Code
- DHA09402122603
Company information
- Manufacturer
- LIFEVAC LLC
- Manufacturer Country
- United States
- Authorized Representative
- LaetusGrace LLC.
Product details
- Intended Use
- Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D6810 Tracheobronchial suction catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 05, 2020
- Expiry Date
- Feb 05, 2025
About this record
Access comprehensive regulatory information for "LifeVac" Tracheobronchial suction catheter (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 4c46b690f3c238512dc170d3358da8b3 and manufactured by LIFEVAC LLC. The authorized representative in Taiwan is LaetusGrace LLC..
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