Taiwan FDA registration 76d1d7ab92f55fa07f573d09c1a8d1d9
“Dr. Plate”Haemophilus Test Medium
TW: “達特普雷”嗜血桿菌試驗培養基
Taiwan·Risk Class 2·MD·DR. PLATE BIOTECH COMPANY·Registered Oct 13, 2015 – Oct 13, 2025ExpiredRegistration details
- Analysis ID
- 76d1d7ab92f55fa07f573d09c1a8d1d9
- License Form
- Ministry of Health Medical Device Manufacturing No. 004956
Company information
- Manufacturer
- DR. PLATE BIOTECH COMPANY
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DR. PLATE BIOTECH COMPANY
Product details
- Intended Use
- Used as a medium for performing Kirby-Bauer antibiotic susceptibility tests. The applicable strain is Haemophilus influenzae.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C1700 Antimicrobial susceptibility test medium
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 13, 2015
- Expiry Date
- Oct 13, 2025
About this record
Access comprehensive regulatory information for “Dr. Plate”Haemophilus Test Medium in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76d1d7ab92f55fa07f573d09c1a8d1d9 and manufactured by DR. PLATE BIOTECH COMPANY. The authorized representative in Taiwan is DR. PLATE BIOTECH COMPANY.
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