Pure Global

“Dr. Plate”Haemophilus Test Medium - Taiwan Registration 76d1d7ab92f55fa07f573d09c1a8d1d9

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.

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 Database
Powered by Pure Global AI
89,000+ Devices
76d1d7ab92f55fa07f573d09c1a8d1d9
Registration Details
Taiwan FDA Registration: 76d1d7ab92f55fa07f573d09c1a8d1d9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Dr. Plate”Haemophilus Test Medium
TW: “達特普雷”嗜血桿菌試驗培養基
Risk Class 2
MD

Registration Details

76d1d7ab92f55fa07f573d09c1a8d1d9

Ministry of Health Medical Device Manufacturing No. 004956

Company Information

Taiwan, Province of China

Product Details

Used as a medium for performing Kirby-Bauer antibiotic susceptibility tests. The applicable strain is Haemophilus influenzae.

C Immunology and microbiology devices

C1700 Antimicrobial susceptibility test medium

Produced in Taiwan, China

Dates and Status

Oct 13, 2015

Oct 13, 2025