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Portable X-Ray System

FDA UDI

Class II (US FDA UDI)

by Konica Minolta Medical Imaging U.s.a., Inc.

Identity

Trade Name
Portable X-Ray System FDA UDI
Generic Name
Portable basic diagnostic x-ray system, digital FDA UDI
Device Name
SR-130 + DR Portable VIZION M portavle X-Ray System (100kV/30mA). FDA UDI
Model / Reference
XR310 FDA UDI
Description
SR-130 + DR Portable VIZION M portavle X-Ray System (100kV/30mA). FDA UDI

Identifiers

Primary DI / UDI-DI
00817100020124 FDA UDI
FDA Product Code
IZL FDA UDI
GMDN Term
Portable basic diagnostic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1720 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

No

FDA UDI

Category: Portable basic diagnostic x-ray system, digital

Portable X-Ray System by Konica Minolta Medical Imaging U.s.a., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable basic diagnostic x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Konica Minolta Medical Imaging U.s.a., Inc.

Sources (1)

  • FDA UDI 86918c2e-6eab-400e-908d-e619f3785ff0 34 fields · synced Jun 1, 2026