Taiwan FDA registration 82624683381b45e9bd165fadba7b5b1a
Feiblikai Limb Equipment (Unsterilized)
TW: 費布力凱汛 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·FABRICATION ENTERPRISES INCORPORATED·Registered Sep 02, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 82624683381b45e9bd165fadba7b5b1a
- Customs Code
- DHA084a0022001
Company information
- Manufacturer
- FABRICATION ENTERPRISES INCORPORATED
- Manufacturer Country
- United States
- Authorized Representative
- Renyu Medical Equipment CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
Dates and status
- Registration Date
- Sep 02, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Feiblikai Limb Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 82624683381b45e9bd165fadba7b5b1a and manufactured by FABRICATION ENTERPRISES INCORPORATED. The authorized representative in Taiwan is Renyu Medical Equipment CO., LTD..
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