Taiwan FDA registration ffde407187f3e5f9221be9d7082479dd
“Zimmer” ZFieldDual Magnetotherapy Device
TW: “利麥爾” 立富多磁波治療器
Taiwan·Risk Class 2·MD·ZIMMER MEDIZINSYSTEME GMBH·Registered May 14, 2021 – May 14, 2026ExpiredRegistration details
- Analysis ID
- ffde407187f3e5f9221be9d7082479dd
- License Form
- Ministry of Health Medical Device Import No. 034528
- Customs Code
- DHA05603452807
Company information
- Manufacturer
- ZIMMER MEDIZINSYSTEME GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WOH MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5850 powered muscle stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 14, 2021
- Expiry Date
- May 14, 2026
About this record
Access comprehensive regulatory information for “Zimmer” ZFieldDual Magnetotherapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ffde407187f3e5f9221be9d7082479dd and manufactured by ZIMMER MEDIZINSYSTEME GMBH. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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