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"Mindray" infusion pump - Taiwan Registration de02bbc3fef493e960139b5d7338ee51

Access comprehensive regulatory information for "Mindray" 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 de02bbc3fef493e960139b5d7338ee51 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.;; Shenzhen Mindray Scientific Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.

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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de02bbc3fef493e960139b5d7338ee51
Registration Details
Taiwan FDA Registration: de02bbc3fef493e960139b5d7338ee51
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Device Details

"Mindray" infusion pump
TW: ๏ผ‚้‚็‘ž๏ผ‚่ผธๆถฒๅนซๆตฆ
Risk Class 2

Registration Details

de02bbc3fef493e960139b5d7338ee51

DHA09200133802

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J.5725 Infusion ๅนซๆตฆ

Chinese goods;; input

Dates and Status

May 26, 2022

May 26, 2027