Taiwan FDA registration 42a9d20adedfdad5ed8144405e82a2bb

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·FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD·Registered Nov 30, 2011 – Nov 30, 2021Cancelled
Registration details
Analysis ID
42a9d20adedfdad5ed8144405e82a2bb
Customs Code
DHA04200041009
Company information
Manufacturer Country
China
Authorized Representative
Sunray Health Limited
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
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
Nov 30, 2011
Expiry Date
Nov 30, 2021
Cancellation Date
Sep 23, 2023
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 42a9d20adedfdad5ed8144405e82a2bb and manufactured by FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HEBEI XINLE SCI&TECH 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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