Taiwan FDA registration fecb9d0247581a35415af8b5c5be5fe1

"K-scope" Operating handlamp (Non-Sterile)

TW: “凱司”手術用頭燈(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·K-SCOPE·Registered Oct 14, 2019 – Oct 14, 2024Expired
Registration details
Analysis ID
fecb9d0247581a35415af8b5c5be5fe1
License Form
Ministry of Health Medical Device Import No. 020943
Customs Code
DHA09402094300
Company information
Manufacturer
K-SCOPE
Manufacturer Country
Korea, Republic of
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Surgical Headlamps (M.4335)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M4335 Surgical headlamp
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 14, 2019
Expiry Date
Oct 14, 2024
Companies making similar products

Top companies providing products similar to ""K-scope" Operating handlamp (Non-Sterile)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "K-scope" Operating handlamp (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 fecb9d0247581a35415af8b5c5be5fe1 and manufactured by K-SCOPE. The authorized representative in Taiwan is Shiang Tai Medical Instructment CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including K-SCOPE, 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations