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"Baiduoli" through tube needle - Taiwan Registration db0b26bf030dfb1d6ca2082305c86597

Access comprehensive regulatory information for "Baiduoli" through tube needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db0b26bf030dfb1d6ca2082305c86597 and manufactured by BIOTRONIC SE & CO. KG. 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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db0b26bf030dfb1d6ca2082305c86597
Registration Details
Taiwan FDA Registration: db0b26bf030dfb1d6ca2082305c86597
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Device Details

"Baiduoli" through tube needle
TW: โ€œ็™พๅคšๅŠ›โ€้€š็ฎก้‡
Risk Class 2

Registration Details

db0b26bf030dfb1d6ca2082305c86597

DHA05603321902

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

E.1380 ๅฐŽ็ฎกๅ…ง้€š็ฎก้‡

import

Dates and Status

Jan 17, 2020

Jan 17, 2030