Taiwan FDA registration 0af7576f069be73d568507a2d27a7585
"Dartprel" Identification Medium (Sterilized)
TW: "達特普雷" 鑑別培養基 (滅菌)
Taiwan·Risk Class 1·DR. PLATE BIOTECH COMPANY·Registered Sep 06, 2013 – Sep 06, 2028ActiveRegistration details
- Analysis ID
- 0af7576f069be73d568507a2d27a7585
Company information
- Manufacturer
- DR. PLATE BIOTECH COMPANY
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DR. PLATE BIOTECH COMPANY
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Identification medium (C.2320)The first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2320 Differential culture media
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Sep 06, 2013
- Expiry Date
- Sep 06, 2028
About this record
Access comprehensive regulatory information for "Dartprel" Identification 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 0af7576f069be73d568507a2d27a7585 and manufactured by DR. PLATE BIOTECH COMPANY. The authorized representative in Taiwan is DR. PLATE BIOTECH COMPANY.
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