Taiwan FDA registration 466238f240d9308f471b76e8c4db0ad7
"Intergra" Ear, nose, and throat fiberoptic light source and carrier (Non-sterile)
TW: "英特格拉" 耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·MD·INTERGRA YORK PA, INC·Registered Aug 25, 2015 – Aug 25, 2025ExpiredRegistration details
- Analysis ID
- 466238f240d9308f471b76e8c4db0ad7
- License Form
- Ministry of Health Medical Device Import No. 015602
- Customs Code
- DHA09401560206
Company information
- Manufacturer
- INTERGRA YORK PA, INC
- Manufacturer Country
- United States
- Authorized Representative
- TRANSMEDIC CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 25, 2015
- Expiry Date
- Aug 25, 2025
About this record
Access comprehensive regulatory information for "Intergra" Ear, nose, and throat fiberoptic light source and carrier (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 466238f240d9308f471b76e8c4db0ad7 and manufactured by INTERGRA YORK PA, INC. The authorized representative in Taiwan is TRANSMEDIC CO., LTD..
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