Taiwan FDA registration 67afdc8b0272642c3bec79c707f67e51
"Telifes" Manual Orthopedic Surgical Instruments (Unsterilized)
TW: “泰利芙斯” 手動式骨科手術器械（未滅菌）
Taiwan·Risk Class 1·Teleflex Medical·Registered Apr 07, 2011 – Apr 07, 2026ExpiredRegistration details
- Analysis ID
- 67afdc8b0272642c3bec79c707f67e51
- Customs Code
- DHA04401015209
Company information
- Manufacturer
- Teleflex Medical
- Manufacturer Country
- United States
- Authorized Representative
- ASIA EAGLE CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- import
Dates and status
- Registration Date
- Apr 07, 2011
- Expiry Date
- Apr 07, 2026
About this record
Access comprehensive regulatory information for "Telifes" Manual Orthopedic Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67afdc8b0272642c3bec79c707f67e51 and manufactured by Teleflex Medical. The authorized representative in Taiwan is ASIA EAGLE 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