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Nx

FDA UDI

Class II (US FDA UDI)

by Agfa Corp.

Identity

Trade Name
NX FDA UDI
Generic Name
Radiology DICOM image processing application software FDA UDI
Device Name
NX 2.0 SOFTWARE FDA UDI
Model / Reference
2.0. FDA UDI
Description
NX 2.0 SOFTWARE FDA UDI

Identifiers

Catalog Number
E1AMX FDA UDI
Primary DI / UDI-DI
05414904217818 FDA UDI
510(k) Number
K141602 FDA UDI
FDA Product Code
MQB FDA UDI
GMDN Term
Radiology DICOM image processing application software 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiology DICOM image processing application software

Nx by Agfa Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiology DICOM image processing application software.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agfa Corp.

Sources (1)

  • FDA UDI d219140a-eb9c-4095-84de-2020de0e0aaf 36 fields · synced May 30, 2026