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BD bone marrow aspiration - Taiwan Registration d07fc8fc83686e4927b1ceec7bebf07e

Access comprehensive regulatory information for BD bone marrow aspiration in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d07fc8fc83686e4927b1ceec7bebf07e and manufactured by BARD PERIPHERAL VASCULAR, INC.;; CAREFUSION 2200, INC.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BARD PERIPHERAL VASCULAR, INC.;; CAREFUSION D.R. 203, LTD., and 1 recent registrations in the same category. 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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d07fc8fc83686e4927b1ceec7bebf07e
Registration Details
Taiwan FDA Registration: d07fc8fc83686e4927b1ceec7bebf07e
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Device Details

BD bone marrow aspiration
TW: BD้ชจ้ซ“ๆŠฝๅ–้‡
Risk Class 2

Registration Details

d07fc8fc83686e4927b1ceec7bebf07e

DHA00601100405

Product Details

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

H Gastroenterology and urology

import

Dates and Status

Jan 13, 2005

Jan 13, 2025

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