Taiwan FDA registration a80a06fa8458f637e0c1c8cb9cc9d5ae

"Intek" Anji Annin Medical Device Equipment Disinfection and Biocide (Unsterilized)

TW: "醫特克" 安除寧 醫療器械設備消毒殺菌劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·E-TECH CO., LTD.·Registered Oct 18, 2012 – Oct 18, 2017Cancelled
Registration details
Analysis ID
a80a06fa8458f637e0c1c8cb9cc9d5ae
Customs Code
DHA04401226404
Company information
Manufacturer
E-TECH CO., LTD.
Manufacturer Country
Japan
Authorized Representative
HIPPOCRATES PHARMA CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.6890 Disinfectants for general medical equipment
Import Information
import
Dates and status
Registration Date
Oct 18, 2012
Expiry Date
Oct 18, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Intek" Anji Annin Medical Device Equipment Disinfection and Biocide (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a80a06fa8458f637e0c1c8cb9cc9d5ae and manufactured by E-TECH CO., LTD.. The authorized representative in Taiwan is HIPPOCRATES PHARMA 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