Taiwan FDA registration 3a6b618229fa4548199b66d8a4a4c833
Dayi Younet insulation lamp
TW: 大億優耐特保溫燈
Taiwan·Risk Class 2·Shiquan Co., Ltd. Zhonghe Factory·Registered Oct 01, 2009 – Oct 01, 2014CancelledRegistration details
- Analysis ID
- 3a6b618229fa4548199b66d8a4a4c833
- Customs Code
- DHY00500280202
Company information
- Manufacturer
- Shiquan Co., Ltd. Zhonghe Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dayi Medical Instrument Factory
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Oct 01, 2009
- Expiry Date
- Oct 01, 2014
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Dayi Younet insulation lamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a6b618229fa4548199b66d8a4a4c833 and manufactured by Shiquan Co., Ltd. Zhonghe Factory. The authorized representative in Taiwan is Dayi Medical Instrument Factory.
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