Taiwan FDA registration 9746d384fafec1b7f0b60b3fc77130ca
"Vitromed" Enriched culture medium (Non-sterile)
TW: "維醫"強化培養基(未滅菌)
Registration details
- Analysis ID
- 9746d384fafec1b7f0b60b3fc77130ca
- License Form
- Ministry of Health Medical Device Import No. 018753
- Customs Code
- DHA09401875303
Company information
- Manufacturer
- VITROMED GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MING-MEI TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Intensive Medium (C.2330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2330 fortified medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 24, 2018
- Expiry Date
- Jan 24, 2023
About this record
Access comprehensive regulatory information for "Vitromed" Enriched 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 9746d384fafec1b7f0b60b3fc77130ca and manufactured by VITROMED GMBH. The authorized representative in Taiwan is MING-MEI 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