Taiwan FDA registration 393bc844ec2670eb828bd3cef7fd6e5c

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Glucose Preservation Tube)

TW: 麥斯特一次性使用真空採血管(氟化鈉)
Taiwan flagTaiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Aug 13, 2014 – Aug 13, 2024Expired
Registration details
Analysis ID
393bc844ec2670eb828bd3cef7fd6e5c
License Form
Ministry of Health Medical Device Import No. 026502
Customs Code
DHA05602650206
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
EAFAN ENTERPRISE CO., LTD.
Product details
Intended Use
Blood collection tubes for blood glucose detection.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1675 Blood Sample Collection Device
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 13, 2014
Expiry Date
Aug 13, 2024
About this record

Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Glucose Preservation Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 393bc844ec2670eb828bd3cef7fd6e5c and manufactured by SOYAGREENTEC 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.

Free DatabasePowered by Pure Global AI89,000+ Devices