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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
6m cable to connect PerkinElmer XRpad Detector to XRpad IPU (Interface Power Unit) FDA UDI
Model / Reference
XRpad LPT Detector Cable 20FT-6M FDA UDI
Description
6m cable to connect PerkinElmer XRpad Detector to XRpad IPU (Interface Power Unit) FDA UDI

Identifiers

Catalog Number
95510929H FDA UDI
Primary DI / UDI-DI
00812589020214 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Dimensions & Sizes

Size
Length — 6 Meter 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a8536c16-52ba-4bbf-8a0d-b77981c1c86e 36 fields · synced May 30, 2026