Taiwan FDA registration b000500541e16d1357052baeb47e437c

Yijia single-use vacuum blood collection (separating gel/coagulant)

TW: 醫佳一次性使用真空採血管(分離膠/促凝劑)
Taiwan flagTaiwan·Risk Class 2·HEBEI XINLE SCI&TECH CO., LTD.·Registered May 12, 2014 – May 12, 2019Cancelled
Registration details
Analysis ID
b000500541e16d1357052baeb47e437c
Customs Code
DHA09200061102
Company information
Manufacturer Country
China
Authorized Representative
AGREE HEALTH CARE TECHNOLOGY, LTD.
Product details
Intended Use
This product can be centrifuged to separate serum and plasma (blood cells) after blood collection, and can be used for serum biochemistry and serum immunology examinations.
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 12, 2014
Expiry Date
May 12, 2019
Cancellation Date
Sep 15, 2017
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for Yijia single-use vacuum blood collection (separating gel/coagulant) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b000500541e16d1357052baeb47e437c and manufactured by HEBEI XINLE SCI&TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD, and 1 recent registrations in the same category. 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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