MaxFilter™ 2.2 SW25613N
by Megin Oy
MaxFilter™ 2.2 SW25613N is a Class II device made by Megin Oy, registered in EUDAMED and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 06430056480046), active as of 22 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number06430056480046 | Date23 Sep 2016 | StatusListed |
| European Union | CE/MDD EUDAMED | Number— | Date— | StatusActive |
Official records
- EUDAMED public site
- AccessGUDID record 06430056480046
Across registries
- EUDAMED Active
- FDA GUDID UDI-DI 06430056480046 listed 23 Sep 2016 Listed
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- MaxFilter™ 2.2
- Generic name
- Electroencephalograph
- Model / reference
- SW25613N
- Primary DI / UDI-DI
- 06430056480046
- FDA product code
- OLY
- GMDN term
- Electroencephalograph
- Device class
- Class II
- Regulation number
- 882.1400
- GUDID distribution status
- In Commercial Distribution
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