Taiwan FDA registration e9e2e3abd1e73e839ab501c4d3fab7df

Single-use vacuum blood collection tubes (dipotassium edtaet)

TW: 醫凡一次性使用真空採血管(乙二胺四乙酸二鉀)

Taiwan·Risk Class 2·HEBEI XINLE SCI & TECH CO., LTD.·Registered Nov 09, 2018 – Nov 09, 2028Active

Registration details

Analysis ID: e9e2e3abd1e73e839ab501c4d3fab7df
Customs Code: DHA09200068900

Company information

Manufacturer: HEBEI XINLE SCI & TECH CO., LTD.
Manufacturer Country: China
Authorized Representative: EAFAN ENTERPRISE CO., LTD.

Product details

Intended Use: This product is used to collect, transport and process blood for plasma or whole blood testing in clinical laboratories.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1675 Blood collection equipment
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Nov 09, 2018
Expiry Date: Nov 09, 2028

About this record

Access comprehensive regulatory information for Single-use vacuum blood collection tubes (dipotassium edtaet) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e9e2e3abd1e73e839ab501c4d3fab7df and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is EAFAN ENTERPRISE 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.