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"Beswell" intravenous indwelling needle - Taiwan Registration 14d0bf0047c3cc9e030a432bd7e06c17

Access comprehensive regulatory information for "Beswell" intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14d0bf0047c3cc9e030a432bd7e06c17 and manufactured by FujianBestway Medical Polymer Corporation. The authorized representative in Taiwan is RI-MING ENTERPRISES 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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14d0bf0047c3cc9e030a432bd7e06c17
Registration Details
Taiwan FDA Registration: 14d0bf0047c3cc9e030a432bd7e06c17
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Device Details

"Beswell" intravenous indwelling needle
TW: โ€œ็™พไป•้Ÿ‹โ€้œ่„ˆ็•™็ฝฎ้‡
Risk Class 2

Registration Details

14d0bf0047c3cc9e030a432bd7e06c17

DHA04200037800

Company Information

Product Details

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

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

Chinese goods;; input

Dates and Status

Jul 18, 2011

Jul 18, 2021