Taiwan FDA registration 497a520ae13f86791c134f99e177b661
“Muller-Omicron” Disinfectant (Non-Sterile)
TW: “穆勒歐彌卡”消毒液 (未滅菌)
Taiwan·Risk Class 1·MD·Muller-Omicron GmbH & Co. KG·Registered Oct 15, 2019 – Oct 15, 2024ExpiredRegistration details
- Analysis ID
- 497a520ae13f86791c134f99e177b661
- License Form
- Ministry of Health Medical Device Import No. 020948
- Customs Code
- DHA09402094800
Company information
- Manufacturer
- Muller-Omicron GmbH & Co. KG
- Manufacturer Country
- Germany
- Authorized Representative
- E.S.T. BIOTECH INC.
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
- Oct 15, 2019
- Expiry Date
- Oct 15, 2024
About this record
Access comprehensive regulatory information for “Muller-Omicron” Disinfectant (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 497a520ae13f86791c134f99e177b661 and manufactured by Muller-Omicron GmbH & Co. KG. The authorized representative in Taiwan is E.S.T. BIOTECH INC..
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