XRpad Digital X-Ray Detector System

FDA UDI

Class II (US FDA UDI)

by PerkinElmer Technologies GmbH & Co. KG

Identity

Trade Name: XRpad Digital X-Ray Detector System FDA UDI
Generic Name: Flat panel x-ray detector integration unit FDA UDI
Device Name: Medical grade power supply with interfaces to integrate a PerkinElmer XRpad detector into an X-ray system FDA UDI
Model / Reference: XRpad IPU FDA UDI
Description: Medical grade power supply with interfaces to integrate a PerkinElmer XRpad detector into an X-ray system FDA UDI

Identifiers

Catalog Number: 95510922H FDA UDI
Primary DI / UDI-DI: 00812589020153 FDA UDI
FDA Product Code: MQB FDA UDI
GMDN Term: Flat panel x-ray detector integration unit 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Width — 311 Millimeter FDA UDI
Length — 230 Millimeter FDA UDI
Height — 60 Millimeter FDA UDI

Category: Flat panel x-ray detector integration unit

XRpad Digital X-Ray Detector System by PerkinElmer Technologies GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flat panel x-ray detector integration unit.

Monarch — Meridian Medical Systems, LLC · Class II
DR 14S G DX-D IMAGING PACKAGE — Agfa Corp. · Class II
Monarch — Meridian Medical Systems, LLC · Class II
Monarch — Meridian Medical Systems, LLC · Class II
Monarch — Meridian Medical Systems, LLC · Class II
XRpad Digital X-Ray Detector System — Perkinelmer, Inc. · Class II
Monarch — Meridian Medical Systems, LLC · Class II
Monarch — Meridian Medical Systems, LLC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: PerkinElmer Technologies GmbH & Co. KG

Sources (1)

FDA UDI 5acf2e56-61b5-4a9a-81f6-9965fe948dff 36 fields · synced May 30, 2026