Taiwan FDA registration 8a80492b53a809aa80c3a3fe6e9027a2

"Reed" finger-type pulse oximeter

TW: “麗德” 手指型脈搏血氧濃度計
Taiwan flagTaiwan·Risk Class 2·LEADTEK RESEARCH, INC.·Registered Oct 30, 2023 – Oct 30, 2028Active
Registration details
Analysis ID
8a80492b53a809aa80c3a3fe6e9027a2
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
EXACTITUDE BIOTECH CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.2700.
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Oct 30, 2023
Expiry Date
Oct 30, 2028
About this record

Access comprehensive regulatory information for "Reed" finger-type pulse oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8a80492b53a809aa80c3a3fe6e9027a2 and manufactured by LEADTEK RESEARCH, INC.. The authorized representative in Taiwan is EXACTITUDE BIOTECH 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