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InfiMed Digital Imaging System, Nexus, RF/DR, Non Varian Digital Receptor

FDA UDI

Class II (US FDA UDI)

by Varex Imaging Corporation

Identity

Trade Name
InfiMed Digital Imaging System, Nexus, RF/DR, Non Varian Digital Receptor FDA UDI
Generic Name
X-ray system computer, diagnostic, general-purpose FDA UDI
Model / Reference
Nexus DRF (RF/DR) FDA UDI

Identifiers

Primary DI / UDI-DI
00854344007078 FDA UDI
510(k) Number
K103416 FDA UDI
FDA Product Code
OWB FDA UDI
MQB FDA UDI
JAA FDA UDI
GMDN Term
X-ray system computer, diagnostic, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 FDA UDI
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

InfiMed Digital Imaging System, Nexus, RF/DR, Non Varian Digital Receptor by Varex Imaging Corporation — Class II — FDA UDI — listed in FDA GUDID

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 3ab27183-28fa-4a7e-a737-616b0d836af7 33 fields · synced Jun 9, 2026