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Xplorer 2200 Digital Radiographic System

FDA UDI

Class II (US FDA UDI)

by Imaging Dynamics Company Ltd

Identity

Trade Name
Xplorer 2200 Digital Radiographic System FDA UDI
Generic Name
Stationary basic diagnostic x-ray system, digital FDA UDI
Device Name
Digital Radiographic System FDA UDI
Model / Reference
2200 X4C FDA UDI
Description
Digital Radiographic System FDA UDI

Identifiers

Primary DI / UDI-DI
00823073061018 FDA UDI
FDA Product Code
KPR FDA UDI
MQB FDA UDI
GMDN Term
Stationary basic diagnostic x-ray system, digital 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
Area/Surface Area — 46000 Square centimeter FDA UDI
Weight — 147 Kilogram FDA UDI
Height — 207 Centimeter FDA UDI
Weight — 267 Kilogram FDA UDI

Category: Stationary basic diagnostic x-ray system, digital

Xplorer 2200 Digital Radiographic System by Imaging Dynamics Company Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Imaging Dynamics Company Ltd

Sources (1)

  • FDA UDI 08cd1094-298b-41db-b327-7f53ea97d2fb 36 fields · synced May 30, 2026