Taiwan FDA registration 6877d71835c0f6805ffb52cb68053578
“Merits” Powerpack for manual wheelchair
TW: “國睦”電動輔助式後輪
Taiwan·Risk Class 2·MD·Guomu Industry Co., Ltd. General Factory·Registered Nov 20, 2018 – Nov 20, 2028ActiveRegistration details
- Analysis ID
- 6877d71835c0f6805ffb52cb68053578
- License Form
- Ministry of Health Medical Device Manufacturing No. 006236
Company information
- Manufacturer
- Guomu Industry Co., Ltd. General Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Guomu Industry Co., Ltd. General Factory
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3860 powered wheelchair
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 20, 2018
- Expiry Date
- Nov 20, 2028
About this record
Access comprehensive regulatory information for “Merits” Powerpack for manual wheelchair in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6877d71835c0f6805ffb52cb68053578 and manufactured by Guomu Industry Co., Ltd. General Factory. The authorized representative in Taiwan is Guomu Industry Co., Ltd. General 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