Taiwan FDA registration b0809d9fbeb1e781ebf1a5455b2763ef
“Mego Afek” compression therapy systems
TW: “美固雅飛克”氣壓治療系統
Taiwan·Risk Class 2·MD·MEGO AFEK ACS LTD.·Registered May 13, 2019 – May 13, 2024ExpiredRegistration details
- Analysis ID
- b0809d9fbeb1e781ebf1a5455b2763ef
- License Form
- Ministry of Health Medical Device Import No. 032606
- Customs Code
- DHA05603260604
Company information
- Manufacturer
- MEGO AFEK ACS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- Yuanhong Instrument Co., Ltd
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)
- O5650 Power Expansion Tubular Massager
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 13, 2019
- Expiry Date
- May 13, 2024
About this record
Access comprehensive regulatory information for “Mego Afek” compression therapy systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0809d9fbeb1e781ebf1a5455b2763ef and manufactured by MEGO AFEK ACS LTD.. The authorized representative in Taiwan is Yuanhong Instrument Co., Ltd.
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