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"Carneka" coronary angioplasty probes the catheter - Taiwan Registration 793241a8532940dea2cf45da6b35d18d

Access comprehensive regulatory information for "Carneka" coronary angioplasty probes the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 793241a8532940dea2cf45da6b35d18d and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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793241a8532940dea2cf45da6b35d18d
Registration Details
Taiwan FDA Registration: 793241a8532940dea2cf45da6b35d18d
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Device Details

"Carneka" coronary angioplasty probes the catheter
TW: "ๅกๅ…งๅก"ๅ† ็‹€ๅ‹•่„ˆๆˆๅž‹่ก“ๆŽขๆธฌๅฐŽ็ฎก
Risk Class 2

Registration Details

793241a8532940dea2cf45da6b35d18d

DHA00601736706

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Oct 23, 2006

Oct 23, 2026