Taiwan FDA registration 681210cf90079917bfe14b570a5113e7

“Leadtek” Fingertip Pulse Oximeter

TW: “麗臺” 手指型脈搏血氧濃度計
Taiwan flagTaiwan·Risk Class 2·MD·LEADTEK RESEARCH, INC.·Registered Mar 31, 2023 – Mar 31, 2028Active
Registration details
Analysis ID
681210cf90079917bfe14b570a5113e7
License Form
Ministry of Health Medical Device Manufacturing No. 007837
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LEADTEK RESEARCH, INC.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E2700 Oximeter
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Mar 31, 2023
Expiry Date
Mar 31, 2028
Companies making similar products

Top companies providing products similar to "“Leadtek” Fingertip Pulse Oximeter"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for “Leadtek” Fingertip 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 681210cf90079917bfe14b570a5113e7 and manufactured by LEADTEK RESEARCH, INC.. The authorized representative in Taiwan is LEADTEK RESEARCH, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Litai Technology Co., Ltd. Zhonghe Second Factory, 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations