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"Bozhi" rapid pregnancy test reagent series - Taiwan Registration 8bdb0cfb5741a02a66129debdd7abbac

Access comprehensive regulatory information for "Bozhi" rapid pregnancy test reagent series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8bdb0cfb5741a02a66129debdd7abbac and manufactured by Primus International Marketing Limited;; Dongyao Biotechnology Co., Ltd. The authorized representative in Taiwan is BOR JYH INTERNATIONAL MARKETING CO., LTD..

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8bdb0cfb5741a02a66129debdd7abbac
Registration Details
Taiwan FDA Registration: 8bdb0cfb5741a02a66129debdd7abbac
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Device Details

"Bozhi" rapid pregnancy test reagent series
TW: โ€œๅšๆ™บโ€ ๅฟซ้€Ÿ้ฉ—ๅญ•่ฉฆๅŠ‘็ณปๅˆ—
Risk Class 2

Registration Details

8bdb0cfb5741a02a66129debdd7abbac

Company Information

Product Details

The urine is tested qualitatively for human chorionic gonadotropin. New performance: Added non-professional use.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Domestic;; Contract manufacturing

Dates and Status

May 19, 2016

Sep 28, 2025