Taiwan FDA registration dc816e25d75c980f581d0061385559e8

Single-use vacuum blood collection (coagulant)

TW: 醫凡一次性使用真空採血管(促凝劑)

Taiwan·Risk Class 2·HEBEI XINLE SCI & TECH CO., LTD.·Registered May 29, 2014 – May 29, 2029Active

Registration details

Analysis ID: dc816e25d75c980f581d0061385559e8
Customs Code: DHA09200061405

Company information

Manufacturer: HEBEI XINLE SCI & TECH CO., LTD.
Manufacturer Country: China
Authorized Representative: AGREE HEALTH CARE TECHNOLOGY, LTD.

Product details

Intended Use: It is used for serum biochemistry (liver function, kidney function, heart function, metabolism, etc.), electrolytes, thyroid function, AIDS monitoring, tumor markers, serum immunological examination of blood collection tubes.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1675 Blood collection equipment
Import Information: Chinese goods;; input

Dates and status

Registration Date: May 29, 2014
Expiry Date: May 29, 2029

About this record

Access comprehensive regulatory information for Single-use vacuum blood collection (coagulant) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc816e25d75c980f581d0061385559e8 and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..

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