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RAMP D-dimer Assay - Taiwan Registration 73323c6332e221e4ffdc5f3fab3e0ac1

Access comprehensive regulatory information for RAMP D-dimer Assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 73323c6332e221e4ffdc5f3fab3e0ac1 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..

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.

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73323c6332e221e4ffdc5f3fab3e0ac1
Registration Details
Taiwan FDA Registration: 73323c6332e221e4ffdc5f3fab3e0ac1
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Device Details

RAMP D-dimer Assay
TW: โ€œๅ€ซๆ™ฎโ€ ็บ–็ถญ่›‹็™ฝๅดฉ่งฃ็”ขๅ“ๅˆ†ๆž่ฉฆๅŠ‘็ต„
Risk Class 2
MD

Registration Details

73323c6332e221e4ffdc5f3fab3e0ac1

Ministry of Health Medical Device Import No. 027885

DHA05602788501

Company Information

Product Details

This product is used for the quantitative detection of human fiber degradation product (FDP) dimer in EDTA anticoagulant whole blood collection blood collection blood collection blood spectrum blood plasma plasma quantitative coagulation blood spectrum blood plasma blood plasma quantitative coagulation blood collection blood plasma This product is an in vitro diagnostic reagent.

B Hematology and pathology devices

B7320 Fibrinogen Fibrinogen Breakdown Product Analysis

Imported from abroad

Dates and Status

Oct 20, 2015

Oct 20, 2025