Taiwan FDA registration cc813a9c06acbaeab5797b181ae3f181
"Limere" magnetic wave therapy device
TW: “利麥爾” 磁波治療器
Taiwan·Risk Class 2·Remed Co., Ltd.; ZIMMER MEDIZINSYSTEME GMBH·Registered Aug 12, 2023 – Aug 12, 2028ActiveRegistration details
- Analysis ID
- cc813a9c06acbaeab5797b181ae3f181
- Customs Code
- DHA05603658108
Company information
- Manufacturer
- Remed Co., Ltd.; ZIMMER MEDIZINSYSTEME GMBH
- Manufacturer Country
- Korea, Republic of;;Germany
- Authorized Representative
- WOH MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5850 5850.
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Aug 12, 2023
- Expiry Date
- Aug 12, 2028
About this record
Access comprehensive regulatory information for "Limere" magnetic wave therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc813a9c06acbaeab5797b181ae3f181 and manufactured by Remed Co., Ltd.; ZIMMER MEDIZINSYSTEME GMBH. The authorized representative in Taiwan is WOH MEDICAL 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