RAMP Myoglobin Assay - Taiwan Registration 636faac0b9b3cce05d330fc8f6396d71
Access comprehensive regulatory information for RAMP Myoglobin Assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 636faac0b9b3cce05d330fc8f6396d71 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
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Device Details
Registration Details
636faac0b9b3cce05d330fc8f6396d71
Ministry of Health Medical Device Import No. 027907
DHA05602790701
Product Details
This product is a quantitative immunochromochromatography method used in conjunction with the RAMP Reader System or RAMP 200 System in vitro diagnostic products for the detection of Myoglabrobin concentration in EDTA whole blood.
C Immunology and microbiology devices
C5680 Myoglobin immunoassay system
Imported from abroad
Dates and Status
Nov 17, 2015
Nov 17, 2025

