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Unified DIY automatic detection series - Taiwan Registration 2dd29036cf952c583c44a415847c5cd5

Access comprehensive regulatory information for Unified DIY automatic detection series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2dd29036cf952c583c44a415847c5cd5 and manufactured by Lianshang Biotechnology Co., Ltd. Wugu Factory. The authorized representative in Taiwan is PRESIDENT PHARMACEUTICAL CORPORATION.

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2dd29036cf952c583c44a415847c5cd5
Registration Details
Taiwan FDA Registration: 2dd29036cf952c583c44a415847c5cd5
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Device Details

Unified DIY automatic detection series
TW: ็ตฑไธ€DIY่‡ชๅ‹•ๆชขๆธฌ็ณปๅˆ—
Risk Class 2
Cancelled

Registration Details

2dd29036cf952c583c44a415847c5cd5

DHY00500205402

Company Information

Taiwan, Province of China

Product Details

Rapid immunoassay was used to detect human placental chorionic gonadal hormone in urine.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

Domestic

Dates and Status

May 16, 2006

May 16, 2011

Nov 01, 2012

Cancellation Information

Logged out

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