Taiwan FDA registration 84b258d7af67e06d5d96ad0a79bc8bd5
“Laerdal” Suction Unit
TW: “洛德”動力式抽吸幫浦
Taiwan·Risk Class 2·MD·LAERDAL MEDICAL AS·Registered Aug 07, 2021 – Aug 07, 2026ActiveRegistration details
- Analysis ID
- 84b258d7af67e06d5d96ad0a79bc8bd5
- License Form
- Ministry of Health Medical Device Import No. 034811
- Customs Code
- DHA05603481102
Company information
- Manufacturer
- LAERDAL MEDICAL AS
- Manufacturer Country
- Norway
- Authorized Representative
- TAIWAN MEDICAL SERVICES CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4780 powered suction pump
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2021
- Expiry Date
- Aug 07, 2026
About this record
Access comprehensive regulatory information for “Laerdal” Suction Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84b258d7af67e06d5d96ad0a79bc8bd5 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices