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"Mindray" anesthesia machine - Taiwan Registration fe20a0da9e528cf81fa0f84d96bb813e

Access comprehensive regulatory information for "Mindray" anesthesia machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe20a0da9e528cf81fa0f84d96bb813e and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Shenzhen Mindray Bio-Medical Electronics Co., Ltd., and 4 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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fe20a0da9e528cf81fa0f84d96bb813e
Registration Details
Taiwan FDA Registration: fe20a0da9e528cf81fa0f84d96bb813e
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Device Details

"Mindray" anesthesia machine
TW: โ€œ้‚็‘žโ€้บป้†‰ๆฉŸ
Risk Class 2
Cancelled

Registration Details

fe20a0da9e528cf81fa0f84d96bb813e

DHA09200078200

Company Information

Product Details

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

D Anesthesiology

D.5160 Anesthesia or analgesic gas supply machine

Input;; Chinese goods

Dates and Status

Aug 31, 2016

Aug 31, 2021

Aug 15, 2023

Cancellation Information

Logged out

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