Taiwan FDA registration 9dedf116f43d3e854b75e19bbda08bd3
Dr. plate Mueller Hinton Agar
TW: 達特普雷米勒亨頓瓊脂培養基
Taiwan·Risk Class 2·MD·DR. PLATE BIOTECH COMPANY·Registered Mar 12, 2014 – Mar 12, 2024ExpiredRegistration details
- Analysis ID
- 9dedf116f43d3e854b75e19bbda08bd3
- License Form
- Ministry of Health Medical Device Manufacturing No. 004454
Company information
- Manufacturer
- DR. PLATE BIOTECH COMPANY
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DR. PLATE BIOTECH COMPANY
Product details
- Intended Use
- This product is a medium used in antibiotic susceptibility testing using the Bauer-Kirby method.
- 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
- Mar 12, 2014
- Expiry Date
- Mar 12, 2024
About this record
Access comprehensive regulatory information for Dr. plate Mueller Hinton Agar in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9dedf116f43d3e854b75e19bbda08bd3 and manufactured by DR. PLATE BIOTECH COMPANY. The authorized representative in Taiwan is DR. PLATE BIOTECH COMPANY.
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