← Back to catalogue

Nexxis

FDA UDI

Class II (US FDA UDI)

by Barco, Inc.

Identity

Trade Name
Nexxis FDA UDI
Generic Name
Operating room audiovisual data/device management system FDA UDI
Device Name
MNA-120 ENC ANA AUDIO AT FDA UDI
Model / Reference
MNA-120 FDA UDI
Description
MNA-120 ENC ANA AUDIO AT FDA UDI

Identifiers

Catalog Number
K9303171A FDA UDI
Primary DI / UDI-DI
05415334000551 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
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

Category: Operating room audiovisual data/device management system

Nexxis by Barco, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room audiovisual data/device management system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Barco, Inc.

Sources (1)

  • FDA UDI ada115b4-2691-4ed8-a553-d03d467e2221 35 fields · synced Jun 8, 2026