Taiwan FDA registration 42af75ff06619aad5cd8edcc595af8d2
Reiko limb equipment (unsterilized)
TW: 麗子肢體裝具(未滅菌)
Taiwan·Risk Class 1·Aimin Eisai Co., Ltd. Plant 2·Registered Apr 20, 2006 – Apr 20, 2016CancelledRegistration details
- Analysis ID
- 42af75ff06619aad5cd8edcc595af8d2
- Customs Code
- DHY04300129602
Company information
- Manufacturer
- Aimin Eisai Co., Ltd. Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Aimin Eisai Co., Ltd. Plant 2
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 20, 2006
- Expiry Date
- Apr 20, 2016
- Cancellation Date
- May 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Reiko limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42af75ff06619aad5cd8edcc595af8d2 and manufactured by Aimin Eisai Co., Ltd. Plant 2. The authorized representative in Taiwan is Aimin Eisai Co., Ltd. Plant 2.
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