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Dragon K in vitro reagent card - Taiwan Registration 18b48e2cf7cf1975f1215efb1e2c5f45

Access comprehensive regulatory information for Dragon K in vitro reagent card in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 18b48e2cf7cf1975f1215efb1e2c5f45 and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is The first factory of Longteng Biotechnology Co., Ltd.

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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18b48e2cf7cf1975f1215efb1e2c5f45
Registration Details
Taiwan FDA Registration: 18b48e2cf7cf1975f1215efb1e2c5f45
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Device Details

Dragon K in vitro reagent card
TW: ้พ้จฐKไป–ๅ‘ฝ้ซ”ๅค–่ฉฆๅŠ‘ๅก
Risk Class 2
Cancelled

Registration Details

18b48e2cf7cf1975f1215efb1e2c5f45

DHY00500246602

Company Information

Product Details

ๅฎšๆ€งๆชขๆธฌไบบๅฐฟๆถฒไธญ็š„K-ไป–ๅ‘ฝๅŠๅ…ถไปฃ่ฌ็”ข็‰ฉ(้–พๅ€ผ100 ng/mL).

A Clinical chemistry and clinical toxicology

A.0001 ่‹ฏ็’ฐๅˆฉๅฎš่ฉฆ้ฉ—็ณป็ตฑ

Domestic

Dates and Status

Oct 01, 2007

Oct 01, 2017

Dec 13, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ