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NOMAD™ handheld X-ray system

FDA UDI

Class II (US FDA UDI)

by Aribex, Inc.

Identity

Trade Name
NOMAD™ handheld X-ray system FDA UDI
Generic Name
Diagnostic x-ray system generator, hand-held FDA UDI
Device Name
Handheld X-ray FDA UDI
Model / Reference
0.850.0000 FDA UDI
Description
Handheld X-ray FDA UDI

Identifiers

Catalog Number
FP 0001 FDA UDI
Primary DI / UDI-DI
EKAV085000000 FDA UDI
510(k) Number
K051795 FDA UDI
FDA Product Code
EHD FDA UDI
GMDN Term
Diagnostic x-ray system generator, hand-held FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1800 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: Diagnostic x-ray system generator, hand-held

NOMAD™ handheld X-ray system by Aribex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diagnostic x-ray system generator, hand-held.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aribex, Inc.

Sources (1)

  • FDA UDI 326bbba8-87eb-4ee6-82b5-435de6445e4f 37 fields · synced May 29, 2026