Taiwan FDA registration 6cc0a0a327376dbbf0b4d430b3d6dc51
“Zimmer”emFieldPro Magnetotherapy Device
TW: “利麥爾”磁波治療器
Taiwan·Risk Class 2·MD·ZIMMER MEDIZINSYSTEME GMBH·Registered Oct 08, 2022 – Oct 08, 2027ActiveRegistration details
- Analysis ID
- 6cc0a0a327376dbbf0b4d430b3d6dc51
- License Form
- Ministry of Health Medical Device Import No. 035965
- Customs Code
- DHA05603596508
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 Physical Medical Sciences
- Product Type (Level 2)
- O5850 powered muscle stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 08, 2022
- Expiry Date
- Oct 08, 2027
About this record
Access comprehensive regulatory information for “Zimmer”emFieldPro 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 6cc0a0a327376dbbf0b4d430b3d6dc51 and manufactured by ZIMMER MEDIZINSYSTEME GMBH. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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