Magnetom Flow.Elite

MAGNETOM Flow.Elite is a 1.5 tesla magnetic resonance imaging system for cross sectional imaging and spectroscopy of the head, body or extremities. The available examinations depend on the…

Registry build 21.09.26

MAGNETOM Flow.Elite is a 1.5 tesla magnetic resonance imaging system for cross sectional imaging and spectroscopy of the head, body or extremities. The available examinations depend on the local coils configured with the system, and a trained physician interprets the images and derived measurements.

The system combines a magnet, gradient system, radiofrequency system, patient table and measurement and reconstruction hardware. Body and local coils support signal acquisition, while syngo MR XB10 software controls the imaging workflow and image reconstruction.

Workflow Controls

The Select&GO touch display supports patient registration, coil based isocenter positioning and scan initiation. MR compatible equipment can also support imaging during interventional procedures, such as use with MR Safe biopsy needles.

12manufacturers in China registered for this device type
1catalogue number
7510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (3), Beijing (2), Guangdong (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LNH
Manufacturer City Province Registered as Device types
Shanghai Chenguang Medical Technologies Co., Ltd. Shanghai Shanghai Contract manufacturer 2
GE Healthcare (China) Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shenzhen Magnetic Resonance Ltd. Shenzhen Guangdong Contract manufacturer 8
GE Healthcare (Tianjin) Company Limited Tianjin Tianjin Specification developer 5
GE Healthcare (China) Co., Ltd. – Tianjin Tianjin Tianjin Specification developer 3
Shenzhen RF Tech Co., Ltd. Shenzhen Guangdong Complaint-file establishment 2
Shanghai Chenshi Medical Instruments Co., Ltd. Shanghai Shanghai Exporter 2
MRI Division, Beijing Wandong Medical Technology Co., Ltd. Beijing Beijing Manufacturer 1
Jiangsu Magspin Instrument Co., Ltd. Kunshan Jiangsu Manufacturer 1
Xingaoyi Medical Equipment Co., Ltd. Yuyao Zhejiang Manufacturer 1
Sino Canada Health Engineering Research Institute (Hefei) Ltd. (Scheri) Hefei Anhui Complaint-file establishment 1

Record

Regulatory record for Magnetom Flow.Elite
Listed by Siemens Healthcare Limited, Canada
FDA product code LNH
Device type System, Nuclear Magnetic Resonance Imaging
Device class Class 2
Regulation 21 CFR 892.1000
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K252838
Record published 2026-01-19

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number

Catalogue Numbers

Catalogue numbers for Magnetom Flow.Elite
Catalogue number Size Status
11851911 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ingenia Philips Medical Systems Nederland B.V. 72
System, Nuclear Magnetic Resonance Imaging GE Medical Systems, L.L.C. 40
System, Nuclear Magnetic Resonance Imaging Medtronic Navigation, Inc. 23
Uni-frame® Thermoplastic Medtec LLC 19
Positioning Cushion Medtec LLC 18
Posicast® Thermoplastic Medtec LLC 18
System, Nuclear Magnetic Resonance Imaging GE Healthcare (Tianjin) Company Limited 16
Invivo Philips DS North America LLC 15
Type-S™ Thermoplastic Medtec LLC 14
Aperto Lucent Fujifilm Corporation 13
MRI Integral “T” with Check Valve for Medrad® Spectris MR Injector Bayer Medical Care Inc. 11
PPG Finger Band IVY Biomedical Systems, Inc. 11

Showing 12 of 478. All products under System, Nuclear Magnetic Resonance Imaging

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252838 2025-12-19
K250443 2025-06-16
K012202 2001-09-27
K994316 2000-01-14
K991652 1999-08-03
K984221 1999-02-12
K984224 1999-02-02

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P860010 1988-06-12 INSTRUMENTARIUM ULF MR IMAGING SYSTEM Palomex Instrumentarium Corp.
P860062 1988-05-25 RESONEX RX4000{TM} MAGNETIC RESONANCE IMAGING SYST Resonex, Inc.
P850043 1987-12-30 MAGNISCAN 5000 MRI SYSTEM Thomson-Cgr Medical Corp.
P830074 1987-11-25 GE SIGNA MAGNETIC RESONANCE DIAGNOSTIC IMAGING SYS General Electric Co.
P840063 1987-08-11 GYROSCAN(TM) Philips Medical Systems Technologies Ltd
P840007 1987-04-02 GYREX, MODELS S3500 & S5000 Elscint, Inc.
P830076 1986-10-08 FONAR NMR WHOLE BODY SCANNER BETA 3000 Fonar Corp.
P830052 1986-05-28 NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000 Philips Medical Systems (Cleveland), Inc.
P830051 1986-04-30 TESLACON(TM) NMR IMAGING SYSTEM Technicare Corp.
P830053 1985-12-18 DIASONICS NMR IMAGING SYSTEM Diasonics, Inc.
P830081 1985-06-06 MAGNETOM Siemens Healthcare Limited

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