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Waters High Pressure Liquid Phase Analysis Instrument for Clinical Use (Unindefatted) - Taiwan Registration 883b4d6833d9bd78b18867e316a61713

Access comprehensive regulatory information for Waters High Pressure Liquid Phase Analysis Instrument for Clinical Use (Unindefatted) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 883b4d6833d9bd78b18867e316a61713 and manufactured by GES Singapore Pte Ltd.;; WATERS CORPORATION. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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883b4d6833d9bd78b18867e316a61713
Registration Details
Taiwan FDA Registration: 883b4d6833d9bd78b18867e316a61713
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Device Details

Waters High Pressure Liquid Phase Analysis Instrument for Clinical Use (Unindefatted)
TW: ๆฒƒ็‰นๆ–ฏ ่‡จๅบŠไฝฟ็”จ็š„้ซ˜ๅฃ“ๆถฒ็›ธๅฑคๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

883b4d6833d9bd78b18867e316a61713

DHA084A0032601

Company Information

United States;;Singapore

Product Details

It is limited to the first level of identification of the classification and grading management of medical devices "high-pressure liquid chromatography instrument for clinical use (A.2260)".

A Clinical chemistry and clinical toxicology

A.2260 High-pressure liquid chromatography for clinical use

Input;; Contract manufacturing

Dates and Status

Nov 28, 2024

Oct 31, 2026