Taiwan FDA registration 56525b8374511346ed2a53804d6d6909
"Askerbien" Fitness Technology Magnetic Wave Stimulator
TW: “阿斯克比恩” 健體科技磁波刺激器
Taiwan·Risk Class 2·DEKA M.E.L.A. S.R.L.·Registered Aug 18, 2024 – Aug 18, 2029ActiveRegistration details
- Analysis ID
- 56525b8374511346ed2a53804d6d6909
- Customs Code
- DHA05603728305
Company information
- Manufacturer
- DEKA M.E.L.A. S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5850 5850.
- Import Information
- import
Dates and status
- Registration Date
- Aug 18, 2024
- Expiry Date
- Aug 18, 2029
About this record
Access comprehensive regulatory information for "Askerbien" Fitness Technology Magnetic Wave Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 56525b8374511346ed2a53804d6d6909 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is QUALTECH CONSULTING 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