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Baxter arteriovenous needles - Taiwan Registration 70331f7a9b9155d81b20f64ead95b683

Access comprehensive regulatory information for Baxter arteriovenous needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 70331f7a9b9155d81b20f64ead95b683 and manufactured by NIPRO (THAILAND) CORPORATION LIMITED. The authorized representative in Taiwan is BAXTER HEALTHCARE 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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70331f7a9b9155d81b20f64ead95b683
Registration Details
Taiwan FDA Registration: 70331f7a9b9155d81b20f64ead95b683
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Device Details

Baxter arteriovenous needles
TW: ็™พ็‰นๅ‹•้œ่„ˆๅป”็ฎก้‡
Risk Class 2
Cancelled

Registration Details

70331f7a9b9155d81b20f64ead95b683

DHA00601832600

Company Information

Product Details

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

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

import

Dates and Status

Sep 14, 2007

Sep 14, 2022

Apr 12, 2024

Cancellation Information

Logged out

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