Taiwan FDA registration 4b9badf02ea25243833f74f9ec4938c6

EV Single-use Containers for Human Venous Blood Specimen Collection(Sterile Heparin Tube)

TW: 醫凡一次性使用真空採血管(肝素鋰)

Taiwan·Risk Class 2·MD·HEBEI XINLE SCI & TECH CO., LTD.·Registered Apr 21, 2014 – Apr 21, 2024Expired

Registration details

Analysis ID: 4b9badf02ea25243833f74f9ec4938c6
License Form: Ministry of Health Medical Device Land Transport No. 000526
Customs Code: DHA09200052608

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 emergency biochemical and plasma biochemical examination.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1675 Blood Sample Collection Device
Import Information: Imported from abroad; Made in China

Dates and status

Registration Date: Apr 21, 2014
Expiry Date: Apr 21, 2024

About this record

Access comprehensive regulatory information for EV Single-use Containers for Human Venous Blood Specimen Collection(Sterile Heparin Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b9badf02ea25243833f74f9ec4938c6 and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..

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