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Streptococcus briboccus grouping rapid latex agglutination kit (unsterilized) - Taiwan Registration 0db74699dfd3ee32e57dfdf5309bc087

Access comprehensive regulatory information for Streptococcus briboccus grouping rapid latex agglutination kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0db74699dfd3ee32e57dfdf5309bc087 and manufactured by PRO-LAB, INC.. The authorized representative in Taiwan is METEK LAB INC..

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0db74699dfd3ee32e57dfdf5309bc087
Registration Details
Taiwan FDA Registration: 0db74699dfd3ee32e57dfdf5309bc087
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Device Details

Streptococcus briboccus grouping rapid latex agglutination kit (unsterilized)
TW: ๆณขๅŠ›ไผฏ้ˆ็ƒ่Œๅˆ†็พคๅฟซ้€Ÿไนณ่† ๅ‡้›†่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0db74699dfd3ee32e57dfdf5309bc087

DHA04400523901

Company Information

Canada

Product Details

Classification and grading management method of medical equipment: Streptococcus belongs to the first level identification range of serum reagent (C.3740).

C Immunology and microbiology

C.3740 ้ˆ็ƒ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Oct 17, 2006

Oct 17, 2026