Taiwan FDA registration 27627673a67b60dff2b431f00e51fa40

"Isolux" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)

TW: "艾萊施"耳鼻喉光纖光源及載具(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ISOLUX LLC·Registered Aug 06, 2014 – Aug 06, 2019Cancelled
Registration details
Analysis ID
27627673a67b60dff2b431f00e51fa40
License Form
Ministry of Health Medical Device Import No. 014414
Customs Code
DHA09401441400
Company information
Manufacturer
ISOLUX LLC
Manufacturer Country
United States
Authorized Representative
KINGJING INTERNATIONAL CO., LTD.
Product details
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 06, 2014
Expiry Date
Aug 06, 2019
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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Access comprehensive regulatory information for "Isolux" 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 27627673a67b60dff2b431f00e51fa40 and manufactured by ISOLUX LLC. The authorized representative in Taiwan is KINGJING INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ISOLUX LLC, and 1 recent registrations in the same category. 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.

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