Taiwan FDA registration 2507cbdfb5662f0a4ec9b80a6c227b3c
"Yanbo" finger-type oximeter
TW: “雃博”手指型血氧濃度計
Taiwan·Risk Class 2·Ruisheng Medical Technology Co., Ltd. Zhubei Factory·Registered Jul 31, 2009 – Jun 05, 2018CancelledRegistration details
- Analysis ID
- 2507cbdfb5662f0a4ec9b80a6c227b3c
- Customs Code
- DHY00500275101
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Wellell Inc.
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.2700.
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jul 31, 2009
- Expiry Date
- Jun 05, 2018
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Yanbo" finger-type oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2507cbdfb5662f0a4ec9b80a6c227b3c and manufactured by Ruisheng Medical Technology Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is Wellell Inc..
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