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"Asahi" does not need a guide tube for percutaneous coronary angioplasty - Taiwan Registration 983a9a63eca233790d89a2b4d3a445aa

Access comprehensive regulatory information for "Asahi" does not need a guide tube for percutaneous coronary angioplasty in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 983a9a63eca233790d89a2b4d3a445aa and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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983a9a63eca233790d89a2b4d3a445aa
Registration Details
Taiwan FDA Registration: 983a9a63eca233790d89a2b4d3a445aa
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Device Details

"Asahi" does not need a guide tube for percutaneous coronary angioplasty
TW: โ€œๆœๆ—ฅโ€็„ก้œ€ๅฐŽๅผ•้ž˜ๆฐดๆผพ็ถ“็šฎๅ† ็‹€ๅ‹•่„ˆๆˆๅž‹่ก“ๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2

Registration Details

983a9a63eca233790d89a2b4d3a445aa

DHA00601876204

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

Apr 01, 2008

Apr 01, 2023