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"Abbott" Esther bedside blood monitor - Taiwan Registration 40053c28cd029e1b673adc06328ba24d

Access comprehensive regulatory information for "Abbott" Esther bedside blood monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 40053c28cd029e1b673adc06328ba24d and manufactured by ABBOTT POINT OF CARE INC.;; Abbott Point of Care Inc.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ABBOTT POINT OF CARE INC.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD, 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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40053c28cd029e1b673adc06328ba24d
Registration Details
Taiwan FDA Registration: 40053c28cd029e1b673adc06328ba24d
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Device Details

"Abbott" Esther bedside blood monitor
TW: โ€œไบžๅŸนโ€่‰พๆ–ฏ็‰นๅบŠๆ—่ก€ๆถฒ็›ฃ่ญทๅ„€
Risk Class 2

Registration Details

40053c28cd029e1b673adc06328ba24d

DHA05603237307

Product Details

Change the performance (adjust the text description) to: This product needs to be equipped with an i-STAT chip cassette, which is used to quantitatively detect various analytes in arterial, venous and microvascular whole blood.

A Clinical chemistry and clinical toxicology

A.1345 Glucose Test System;; A.1145 Calcium testing system;; A.1770 Urea nitrogen test system

Contract manufacturing;; input

Dates and Status

Mar 14, 2019

Mar 14, 2029

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