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"Baidoli" Enoff controlled sheath tube - Taiwan Registration 2c1837e0988f48db1b3e51ee6176e25b

Access comprehensive regulatory information for "Baidoli" Enoff controlled sheath tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2c1837e0988f48db1b3e51ee6176e25b and manufactured by ACUTUS MEDICAL, INC. The authorized representative in Taiwan is BIOTRONIK TAIWAN 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.

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2c1837e0988f48db1b3e51ee6176e25b
Registration Details
Taiwan FDA Registration: 2c1837e0988f48db1b3e51ee6176e25b
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Device Details

"Baidoli" Enoff controlled sheath tube
TW: "็™พๅคšๅŠ›"่‰พ่ซพ่Š™ๅฏๆŽงๅผ้ž˜็ฎก
Risk Class 2

Registration Details

2c1837e0988f48db1b3e51ee6176e25b

DHA05603533004

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1280 controllable guide

import

Dates and Status

Mar 17, 2022

Mar 17, 2027