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RAMP Cardiac Controls - Taiwan Registration 502eeecad7716a23381d883bc5576020

Access comprehensive regulatory information for RAMP Cardiac Controls in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 502eeecad7716a23381d883bc5576020 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..

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502eeecad7716a23381d883bc5576020
Registration Details
Taiwan FDA Registration: 502eeecad7716a23381d883bc5576020
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Device Details

RAMP Cardiac Controls
TW: ๅ€ซๆ™ฎๅฟƒ่‡Ÿๆจ™่จ˜ๅ“็ฎกๆถฒ
Risk Class 2
MD

Registration Details

502eeecad7716a23381d883bc5576020

Ministry of Health Medical Device Import No. 027699

DHA05602769904

Company Information

Product Details

This product is used in the RAMP platform as a quality control of in vitro diagnostic cardiac markers.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Oct 01, 2015

Oct 01, 2025