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OC-Calibrator 2 kit - Taiwan Registration f5d2b9a2f6f1bbc6396cbbdb3304f98b

Access comprehensive regulatory information for OC-Calibrator 2 kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5d2b9a2f6f1bbc6396cbbdb3304f98b and manufactured by EIKEN CHEMICAL CO., LTD. NASU PLANT. The authorized representative in Taiwan is HUI SHENG INTERNATIONAL CORP..

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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f5d2b9a2f6f1bbc6396cbbdb3304f98b
Registration Details
Taiwan FDA Registration: f5d2b9a2f6f1bbc6396cbbdb3304f98b
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Device Details

OC-Calibrator 2 kit
TW: "ๆฆฎ็ ”"ๅ…็–ซๆณ•ไพฟไธญ่ก€็ด…็ด ๅฎš้‡ๅˆ†ๆž็ณป็ตฑ-ๆ กๆญฃ็ต„2
Risk Class 2
MD

Registration Details

f5d2b9a2f6f1bbc6396cbbdb3304f98b

Ministry of Health Medical Device Import No. 033468

DHA05603346800

Company Information

Product Details

This product is a calibration solution for the determination of heme (Hb) in stool using an immunochemical automated analysis instrument. The reagent for the product is "Eiken" OC-AUTO 3.

A Clinical chemistry and clinical toxicology

A1150 calibrate

Imported from abroad

Dates and Status

Apr 09, 2020

Apr 09, 2025