Taiwan FDA registration d8beb53ceeb1e93f1608aaf5273adf56
Huiyuan selective medium (sterilized)
TW: 惠碁選擇性培養基(滅菌)
Registration details
- Analysis ID
- d8beb53ceeb1e93f1608aaf5273adf56
Company information
- Manufacturer
- DR. PLATE BIOTECH COMPANY
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- EUMED BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical devices "Selective culture medium (C.2360)" first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2360 選擇性培養基
- Import Information
- 委託製造;; QMS/QSD;; 國產
Dates and status
- Registration Date
- Apr 29, 2021
- Expiry Date
- Apr 29, 2026
About this record
Access comprehensive regulatory information for Huiyuan selective medium (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d8beb53ceeb1e93f1608aaf5273adf56 and manufactured by DR. PLATE BIOTECH COMPANY. The authorized representative in Taiwan is EUMED BIOTECHNOLOGY 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