Taiwan FDA registration e9249bc10228f66dff2d88d7d5ad7c64
"Liofilchem" Selective culture medium (Non-Sterile)
TW: "利奧菲森" 選擇性培養基 (未滅菌)
Registration details
- Analysis ID
- e9249bc10228f66dff2d88d7d5ad7c64
- License Form
- Ministry of Health Medical Device Import No. 021367
- Customs Code
- DHA09402136708
Company information
- Manufacturer
- LIOFILCHEM S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DiaTech Technology Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Selective Media (C.2360)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2360 selective medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 16, 2020
- Expiry Date
- Mar 16, 2025
About this record
Access comprehensive regulatory information for "Liofilchem" Selective culture medium (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 e9249bc10228f66dff2d88d7d5ad7c64 and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DiaTech Technology 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