“Leadtek” Fingertip Pulse Oximeter
Taiwan·Risk Class 2·MD·Litai Technology Co., Ltd. Zhonghe Second Factory·Registered Sep 26, 2017 – Sep 26, 2027Active- Analysis ID
- b629f5c6ead28070a6dd3e3a8f719d36
- License Form
- Ministry of Health Medical Device Manufacturing No. 005876
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LEADTEK RESEARCH, INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2700 Oximeter
- Import Information
- Produced in Taiwan, China
- Registration Date
- Sep 26, 2017
- Expiry Date
- Sep 26, 2027
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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 b629f5c6ead28070a6dd3e3a8f719d36 and manufactured by Litai Technology Co., Ltd. Zhonghe Second Factory. The authorized representative in Taiwan is LEADTEK RESEARCH, INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LEADTEK RESEARCH, INC., 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.