Taiwan FDA registration 02e381334c78386e41acbe4ba5a5a929
"L&R" General purpose disinfectants (Non-Sterile)
TW: "樂瑞" 一般醫療器械用消毒劑 (未滅菌)
Registration details
- Analysis ID
- 02e381334c78386e41acbe4ba5a5a929
- License Form
- Ministry of Health Medical Device Import No. 019267
- Customs Code
- DHA09401926702
Company information
- Manufacturer
- L&R MANUFACTURING COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- KOLN BIO-MEDICAL 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)
- J6890 Disinfectants for general medical devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 04, 2018
- Expiry Date
- Jul 04, 2023
About this record
Access comprehensive regulatory information for "L&R" General purpose disinfectants (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 02e381334c78386e41acbe4ba5a5a929 and manufactured by L&R MANUFACTURING COMPANY. The authorized representative in Taiwan is KOLN BIO-MEDICAL 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