Taiwan FDA registration 78009a867f059addd2a0e52ad9ab05ee
"Lyfeite" 體外limb體羔義lim用組件 (未滅bacteria)
TW: "萊飛特" 體外肢體義肢用組件 (未滅菌)
Taiwan·Risk Class 1·Levitate Technology ApS·Registered Dec 24, 2024 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 78009a867f059addd2a0e52ad9ab05ee
- Customs Code
- DHA084A0034301
Company information
- Manufacturer
- Levitate Technology ApS
- Manufacturer Country
- Denmark
- Authorized Representative
- TEH LIN PROSTHETIC & ORTHOPAEDIC INC.
Product details
- Intended Use
- It is limited to the first-level identification scope of the components for extracorporeal limb prosthetics (O.3420) of medical equipment classification and hierarchical management.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3420 體外肢體義肢用組件
- Import Information
- import
Dates and status
- Registration Date
- Dec 24, 2024
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Lyfeite" 體外limb體羔義lim用組件 (未滅bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 78009a867f059addd2a0e52ad9ab05ee and manufactured by Levitate Technology ApS. The authorized representative in Taiwan is TEH LIN PROSTHETIC & ORTHOPAEDIC INC..
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