Pure Global

"Remon" fibrin/fibrinogen lysate detection kit - Taiwan Registration c0c3cf844038eb8343e29c05aad545a1

Access comprehensive regulatory information for "Remon" fibrin/fibrinogen lysate detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c0c3cf844038eb8343e29c05aad545a1 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

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
c0c3cf844038eb8343e29c05aad545a1
Registration Details
Taiwan FDA Registration: c0c3cf844038eb8343e29c05aad545a1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Remon" fibrin/fibrinogen lysate detection kit
TW: "้Šณ็›Ÿ" ็บ–็ถญ่›‹็™ฝ/็บ–็ถญ่›‹็™ฝๅŽŸ่ฃ‚่งฃ็”ข็‰ฉๆชขๆธฌๅฅ—็ต„
Risk Class 2
Cancelled

Registration Details

c0c3cf844038eb8343e29c05aad545a1

DHA00601597802

Company Information

United Kingdom

Product Details

Rapid semi-quantitative determination of fibrin/fibrinogen cleavage products (FDP) in human serum and urine samples.

B Hematology, pathology, and genetics

B.7320 Fibrinogen/Fibrinolysis Product Analysis

import

Dates and Status

Feb 09, 2006

Feb 09, 2016

Jan 20, 2017

Cancellation Information

Logged out

็”ณๅพฉ็ถ“ๆ ธไธๅ‡†