Taiwan FDA registration fa43aefc5f0064efeaeced444f70d98a
"Paulette" physiological monitor
TW: “寶萊特”生理監視器
Registration details
- Analysis ID
- fa43aefc5f0064efeaeced444f70d98a
- Customs Code
- DHA09200074303
Company information
- Manufacturer
- Guangdong Biolight Meditech Co., Ltd
- Manufacturer Country
- China
- Authorized Representative
- SUNRISEMEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2300 Cardiac monitor (including cardiac data and heart rate monitor)
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Feb 03, 2016
- Expiry Date
- Feb 03, 2026
About this record
Access comprehensive regulatory information for "Paulette" physiological monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa43aefc5f0064efeaeced444f70d98a and manufactured by Guangdong Biolight Meditech Co., Ltd. The authorized representative in Taiwan is SUNRISEMEDICAL 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