Taiwan FDA registration 5eb80f2fed6a2eaabcc0b436d6f4862f
"Eijima" ENT fiber optic light source and vehicle (unsterilized)
TW: “永島”耳鼻喉光纖光源及載具 (未滅菌)
Registration details
- Analysis ID
- 5eb80f2fed6a2eaabcc0b436d6f4862f
- Customs Code
- DHA04400774704
Company information
- Manufacturer
- NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- FU TAI TRADING 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 Science
- Product Type (Level 2)
- G.4350 Ear, nose and throat optical fiber light sources and carriers
- Import Information
- import
Dates and status
- Registration Date
- May 20, 2009
- Expiry Date
- May 20, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Eijima" ENT fiber optic light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5eb80f2fed6a2eaabcc0b436d6f4862f and manufactured by NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is FU TAI TRADING 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