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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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636faac0b9b3cce05d330fc8f6396d71
Registration Details
Taiwan FDA Registration: 636faac0b9b3cce05d330fc8f6396d71
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Device Details

RAMP Myoglobin Assay
TW: โ€œๅ€ซๆ™ฎโ€ ่‚Œ็ด…่›‹็™ฝๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2
MD

Registration Details

636faac0b9b3cce05d330fc8f6396d71

Ministry of Health Medical Device Import No. 027907

DHA05602790701

Company Information

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