Taiwan FDA registration 122cedca31c69b1b73420c8983e98b9e
"Dartprel" Bactericulture Medium (Sterilized)
TW: "達特普雷" 集菌培養基 (滅菌)
Registration details
- Analysis ID
- 122cedca31c69b1b73420c8983e98b9e
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 first level identification range of the "Intensive Medium (C.2330)" of the Measures for the Classification and Grading Management of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2330 Enhanced culture medium
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Sep 06, 2013
- Expiry Date
- Sep 06, 2028
About this record
Access comprehensive regulatory information for "Dartprel" Bactericulture 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 122cedca31c69b1b73420c8983e98b9e 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