Taiwan FDA registration 5431540f5cb29cd3aa1c0b55c482c840

"Bode" Sdeljeter general medical device disinfectant (unsterilized)

TW: “博德”斯德爾潔特一般醫療器械用消毒劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·BODE CHEMIE GMBH·Registered Oct 19, 2012 – Oct 19, 2017Cancelled
Registration details
Analysis ID
5431540f5cb29cd3aa1c0b55c482c840
Customs Code
DHA04401228104
Company information
Manufacturer
BODE CHEMIE GMBH
Manufacturer Country
Germany
Authorized Representative
MEDIBIOT 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 19, 2012
Expiry Date
Oct 19, 2017
Cancellation Date
Dec 20, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "Bode" Sdeljeter general medical device disinfectant (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5431540f5cb29cd3aa1c0b55c482c840 and manufactured by BODE CHEMIE GMBH. The authorized representative in Taiwan is MEDIBIOT 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