Taiwan FDA registration 4f60cf5f6e43751c853c4cc73075d02f
"Telifes" ENT Manual Surgical Instruments (Unsterilized)
TW: "泰利芙斯" 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·Teleflex Medical·Registered Apr 07, 2011 – Apr 07, 2026ExpiredRegistration details
- Analysis ID
- 4f60cf5f6e43751c853c4cc73075d02f
- Customs Code
- DHA04401015005
Company information
- Manufacturer
- Teleflex Medical
- Manufacturer Country
- United States
- Authorized Representative
- ASIA EAGLE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method for medical equipment "ENT Manual Surgical Instruments (G.4420)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4420 Otolaryngology manual surgical instruments
- 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" ENT Manual 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 4f60cf5f6e43751c853c4cc73075d02f and manufactured by Teleflex Medical. The authorized representative in Taiwan is ASIA EAGLE CO., LTD..
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