Identity
- Trade Name
- Nexxis FDA UDI
- Generic Name
- Operating room audiovisual data/device management system FDA UDI
- Device Name
- MNT-120 H.264 KS FDA UDI
- Model / Reference
- MNT-120 FDA UDI
- Description
- MNT-120 H.264 KS FDA UDI
Identifiers
- Catalog Number
- K9303081A FDA UDI
- Primary DI / UDI-DI
- 05415334000810 FDA UDI
- FDA Product Code
- DXJ FDA UDI
- GMDN Term
- Operating room audiovisual data/device management system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2450 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Nexxis by Barco, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Barco, Inc.
Sources (1)
- FDA UDI e3717924-45fb-4be8-99b2-ec5da112c8a8 36 fields · synced May 30, 2026