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Varex Digital Imaging Software, Nexus, DR, v3.2

FDA UDI

Class II (US FDA UDI)

by Varex Imaging Corporation

Identity

Trade Name
Varex Digital Imaging Software, Nexus, DR, v3.2 FDA UDI
Generic Name
X-ray system computer, diagnostic, general-purpose FDA UDI
Model / Reference
Nexus, DR, v3.2 FDA UDI

Identifiers

Primary DI / UDI-DI
00854344007184 FDA UDI
510(k) Number
K172951 FDA UDI
FDA Product Code
MQB FDA UDI
GMDN Term
X-ray system computer, diagnostic, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 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: X-ray system computer, diagnostic, general-purpose

Varex Digital Imaging Software, Nexus, DR, v3.2 by Varex Imaging Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray system computer, diagnostic, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Varex Imaging Corporation

Sources (1)

  • FDA UDI 0643bb17-a918-4bbe-a6ec-05cee8a4cf5c 33 fields · synced Jun 9, 2026