Taiwan FDA registration 8a80492b53a809aa80c3a3fe6e9027a2
"Reed" finger-type pulse oximeter
TW: “麗德” 手指型脈搏血氧濃度計
Registration details
- Analysis ID
- 8a80492b53a809aa80c3a3fe6e9027a2
Company information
- Manufacturer
- LEADTEK RESEARCH, INC.
- 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