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"Termao" infusion pump - Taiwan Registration 66d4f8e588e757a75fe1769b1a3bf453

Access comprehensive regulatory information for "Termao" infusion pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66d4f8e588e757a75fe1769b1a3bf453 and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION, 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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66d4f8e588e757a75fe1769b1a3bf453
Registration Details
Taiwan FDA Registration: 66d4f8e588e757a75fe1769b1a3bf453
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Device Details

"Termao" infusion pump
TW: โ€œๆณฐ็ˆพ่Œ‚โ€่ผธๆถฒๅนซๆตฆ
Risk Class 2

Registration Details

66d4f8e588e757a75fe1769b1a3bf453

DHA05602614600

Company Information

Product Details

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

J General hospital and personal use equipment

J.5725 Infusion ๅนซๆตฆ

import

Dates and Status

May 12, 2014

May 12, 2029

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