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"TERUMO" RADIFOCUS INTRODUCER II - Taiwan Registration 81a0d0a6ab71f37a2897e3fdcd255b21

Access comprehensive regulatory information for "TERUMO" RADIFOCUS INTRODUCER II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81a0d0a6ab71f37a2897e3fdcd255b21 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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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81a0d0a6ab71f37a2897e3fdcd255b21
Registration Details
Taiwan FDA Registration: 81a0d0a6ab71f37a2897e3fdcd255b21
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Device Details

"TERUMO" RADIFOCUS INTRODUCER II
TW: ่ก€็ฎกๆ”ๅฝฑๅผ•ๅฐŽๅฅ—
Risk Class 2
MD

Registration Details

81a0d0a6ab71f37a2897e3fdcd255b21

Department of Health Medical Device Import No. 007391

DHA00600739100

Company Information

Product Details

0600 Intensive care unit and cardiac intensive monitoring

Imported from abroad

Dates and Status

Dec 15, 1994

Feb 09, 2029