Identity
- Trade Name
- MaxFilter™ 2.2 FDA UDI
- Generic Name
- Electroencephalograph FDA UDI
- Device Name
- MaxFilter™ is used with Elekta Neuromag®, Elekta Neuromag® TRIUX and TRIUX™ neo in suppressing magnetic interference and in reducing measurement artifacts. FDA UDI
- Model / Reference
- SW25613N FDA UDI
- Description
- MaxFilter™ is used with Elekta Neuromag®, Elekta Neuromag® TRIUX and TRIUX™ neo in suppressing magnetic interference and in reducing measurement artifacts. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06430056480046 FDA UDI
- FDA Product Code
- OLY FDA UDI
- GMDN Term
- Electroencephalograph FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electroencephalograph
MaxFilter™ 2.2 by Megin Oy — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Megin Oy
Sources (2)
- FDA UDI 61a6c685-895b-4052-a3f6-47f2e0aacdaa 33 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 4, 2026