FDR Cross

The FDR Cross DR-XD 3000 is a mobile C-arm imaging system with a detachable flat-panel detector. It provides pulsed fluoroscopy and digital radiography for diagnostic, interventional and…

Registry build 21.09.26

The FDR Cross DR-XD 3000 is a mobile C-arm imaging system with a detachable flat-panel detector. It provides pulsed fluoroscopy and digital radiography for diagnostic, interventional and surgical procedures in adults and children.

The C-arm positions the X-ray source and detector for image acquisition. Console, control-cabinet and X-ray-controller software coordinate imaging, with fluoroscopic functionality added to the detector-based radiography arrangement.

Listed Item

The DR-XD 3000 is a mobile C-arm system with detachable flat panel detector, which is intended for use in providing medical imaging for general populations including pediatrics. The device provides pulsed fluoroscopic imaging of patients during diagnostic, interventional and surgical procedures and digital radiographic imaging. It is intended for use in procedures such as holangiography, endoscopic, urologic, orthopedic, neurologic, critical care, peripheral vascular, emergency room procedures. This device does not support cardiac procedures and is not intended for use in performing mammography.

Procedure Scope

Applications include orthopaedic, urological, endoscopic, neurological and peripheral vascular procedures. The system does not support cardiac procedures and is not intended for mammography.

5manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Beijing (2), Shanghai (2), Guangdong (1).

Chinese manufacturers registered for FDA product code OWB
Manufacturer City Province Registered as Device types
GE Hangwei Medical Systems Co., Ltd. Beijing Beijing Specification developer 22
GE Healthcare (China) Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shanghai, Medical Equipment Ltd. Shanghai Shanghai Contract manufacturer 10
Siemens Shenzhen Magnetic Resonance Ltd. Shenzhen Guangdong Contract manufacturer 8

Record

Regulatory record for FDR Cross
Listed by Fujifilm Corporation, Japan
FDA product code OWB
Device type Interventional Fluoroscopic X-Ray System
Device class Class 2
Regulation 21 CFR 892.1650
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K212956
Record published 2021-12-28
Record revised 2024-05-30 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment temperature 15 to 30 °C; Handling environment humidity 15 to 80 % RH; Handling environment atmospheric pressure 70 to 106 KiloPascal; Storage environment temperature -10 to 50 °C; Storage environment humidity 10 to 90 % RH; Storage environment atmospheric pressure 70 to 106 KiloPascal

Catalogue Numbers

Catalogue numbers for FDR Cross
Catalogue number Size Status
DR-XD 3000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
TrackX Trackx Technology Inc. 86
Trinias Shimadzu Corp. 54
Allura Xper FD Philips Medical Systems Nederland B.V. 21
Azurion Philips Medical Systems Nederland B.V. 19
LessRay Nuvasive, Inc. 16
Intelli-C Accessory Nrt – Nordisk Røntgen Teknik A/S 13
Pulse Nuvasive, Inc. 12
O-ARM® Medtronic Navigation, Inc. 11
Genoray Genoray Co., Ltd. 10
Fujifilm Healthcare Americas Corporation A.T.S. Applicazione Tecnologie Speciali SRL 7
Fujifilm Medical Systems U.S.A. Inc. A.T.S. Applicazione Tecnologie Speciali SRL 6
Stephanix A.T.S. Applicazione Tecnologie Speciali SRL 6

Showing 12 of 122. All products under Interventional Fluoroscopic X-Ray System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K212956 2021-11-08

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer