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“RMS” Precision Flow Rate Tubing Set - Taiwan Registration baaa0ca1c2b9e8e0639f95f51553c9c3

Access comprehensive regulatory information for “RMS” Precision Flow Rate Tubing Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number baaa0ca1c2b9e8e0639f95f51553c9c3 and manufactured by Repro-Med Systems, Inc. dba KORU Medical Systems. The authorized representative in Taiwan is GIRAFFES PHARMACEUTICAL COMPANY 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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baaa0ca1c2b9e8e0639f95f51553c9c3
Registration Details
Taiwan FDA Registration: baaa0ca1c2b9e8e0639f95f51553c9c3
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Device Details

“RMS” Precision Flow Rate Tubing Set
TW: “瑞普”普立森流速管
Risk Class 2
MD

Registration Details

baaa0ca1c2b9e8e0639f95f51553c9c3

Ministry of Health Medical Device Import No. 033031

DHA05603303100

Company Information

Product Details

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

J General hospital and personal use equipment

J5440 Intravascular infusion sleeve

Imported from abroad

Dates and Status

Nov 14, 2019

Nov 14, 2024