Taiwan FDA registration ce3f53f0e3a04d638cf55ce4dae10eae
Components for the "Oso" upper limb prosthesis (unsterilized)
TW: “奧索”上肢義肢用組件(未滅菌)
Registration details
- Analysis ID
- ce3f53f0e3a04d638cf55ce4dae10eae
- Customs Code
- DHA08401985800
Company information
- Manufacturer
- Ossur Americas, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- TEH LIN PROSTHETIC & ORTHOPAEDIC INC.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, in vitro limb prosthetic components (O.3420) the first level recognition range.
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Components for the "Oso" upper limb prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ce3f53f0e3a04d638cf55ce4dae10eae and manufactured by Ossur Americas, Inc.. The authorized representative in Taiwan is TEH LIN PROSTHETIC & ORTHOPAEDIC INC..
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