MR 7700

MR 7700 extends the gradient and RF designs with extreme gradient performance to deliver superb image quality in diffusion and neuro-science, improve patient handling setup time, combined…

Registry build 21.09.26

MR 7700 extends the gradient and RF designs with extreme gradient performance to deliver superb image quality in diffusion and neuro-science, improve patient handling setup time, combined with accelerations in 2D- and 3D scanning.

12manufacturers in China registered for this device type
7catalogue numbers in this listing
27510(k) clearances naming this product code
40recalls on this 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 MR 7700
Listed by Philips Medical Systems Nederland B.V., Netherlands
FDA product code LNH
Device type System, Nuclear Magnetic Resonance Imaging
Device class Class 2
Regulation 21 CFR 892.1000
Establishment Contract manufacturer, Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2024-06-19
Record revised 2025-12-15 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries serial number
Storage Handling environment atmospheric pressure 70 to 106 KiloPascal; Handling environment humidity 20 to 95 % RH; Handling environment temperature -20 to 50 °C

Catalogue Numbers

Catalogue numbers for MR 7700
Catalogue number Size Status
MR 7700 In distribution
SmartPath to MR 7700 In distribution
SmartPath to MR 7700 In distribution
Upgrade to MR 7700 In distribution
SmartPath to MR 7700 In distribution
Upgrade to MR 7700 In distribution
Upgrade to MR 7700 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
K253648 2026-02-23
K251808 2025-07-11
K251397 2025-06-04
K232030 2023-08-02
K230972 2023-04-28
K223458 2023-04-06
K213583 2022-05-16
K213516 2022-03-03
K212673 2021-11-19
K193215 2020-04-10
K190461 2019-06-04
K183063 2019-02-14
K181479 2018-08-03
K173079 2018-04-04
K173451 2018-03-20
K173356 2018-03-06
K172920 2018-01-22
K162931 2017-01-06
K163116 2017-01-06
K162940 2016-12-30
K143253 2015-04-09
K140666 2014-06-13
K133526 2014-02-12
K131241 2013-08-30
K102344 2010-11-09
K052078 2005-09-07
K052013 2005-08-02

Recalls

40 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 14 units (All OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 26 units (7 US, 19 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 6 units (4 US, 2 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 3 units OUS
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 103 units (37 US, 66 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 34 units (32 US, 2 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 12 units (2 US, 10 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 376 units (37 US, 339 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 37 units (3 US, 34 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 26 units (All OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 12 units (5 US, 7 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 23 units (10 US, 13 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 121 units (51 US, 70 OUS)
2025-03-24 Class II Process control The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lace 4 units OUS
2019-03-25 Class II Device Design Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks to personnel servicing the MED, MDD or connected cabling. 4 units 2020-06-04
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19
2018-12-21 Class II Unknown/Undetermined by firm There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. 11226 total 2020-11-19

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