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"Abbott" Esther bedside blood monitor - Taiwan Registration c24e22f95af58ec35686ad35f6664500

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 c24e22f95af58ec35686ad35f6664500 and manufactured by ABBOTT POINT OF CARE INC.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD. 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.;; Abbott Point of Care Inc., 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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c24e22f95af58ec35686ad35f6664500
Registration Details
Taiwan FDA Registration: c24e22f95af58ec35686ad35f6664500
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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

c24e22f95af58ec35686ad35f6664500

DHA05602790201

Product Details

Equipped with Abbott special chip cassette, the components in whole blood samples are quantitatively measured.

A Clinical chemistry and clinical toxicology

A.1120 ่ก€ๅ…งๆฐฃ้ซ”(PCO2,PO2)ๅŠ่ก€ๆถฒpHๅ€ผ่ฉฆ้ฉ—็ณป็ตฑ

Input;; Contract manufacturing

Dates and Status

Nov 05, 2015

Nov 05, 2025

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