Somatom Emotion 16 Slice (DE)

Catalogue number 10046789, listed by Siemens Healthcare Limited, Canada, under System, X-Ray, Tomography, Computed. 8 manufacturers in China are registered for this product code.

Registry build 21.09.26
8manufacturers in China registered for this device type
1catalogue number
14510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (2), Shanghai (2), Jiangsu (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JAK
Manufacturer City Province Registered as Device types
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Qisda Electronics (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
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
Neusoft Medical Systems Co., Ltd. Shenyang Liaoning Manufacturer 1
Philips Health Technology (China) Co., Ltd. Shenyang Branch Shenyang Liaoning Specification developer 1

Record

Regulatory record for Somatom Emotion 16 Slice (DE)
Listed by Siemens Healthcare Limited, Canada
FDA product code JAK
Device type System, X-Ray, Tomography, Computed
Device class Class 2
Regulation 21 CFR 892.1750
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K050297
Record published 2016-09-24
Record revised 2021-11-17 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number
Storage Storage environment atmospheric pressure 70 to 106 KiloPascal; Handling environment atmospheric pressure 70 to 106 KiloPascal; Handling environment humidity 10 to 90 % RH; Storage environment temperature -20 to 50 °C; Handling environment temperature -20 to 50 °C; Storage environment humidity 10 to 90 % RH

Catalogue Numbers

Catalogue numbers for Somatom Emotion 16 Slice (DE)
Catalogue number Size Status
10046789 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Visicoil IZI Medical Products LLC 48
Visicoil MR IZI Medical Products LLC 41
Illumisite Covidien LP 25
Imbio LDA Imbio, LLC 24
Edge Covidien LP 20
Revolution GE Hangwei Medical Systems Co., Ltd. 20
Gold Fiducial IZI Medical Products LLC 20
superDimension Covidien LP 17
Lodox Lodox Systems (PTY) Ltd. 12
Revolution GE Medical Systems, L.L.C. 12
Toshiba Scanner Canon Inc. 10
syngo.CT Dual Energy Siemens Healthcare Limited 7

Showing 12 of 495. All products under System, X-Ray, Tomography, Computed

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233753 2024-03-21
K213713 2022-08-11
K170221 2017-04-21
K110366 2011-04-12
K071310 2007-06-08
K063507 2006-11-30
K053024 2005-11-04
K050867 2005-04-14
K991600 1999-06-09
K984634 1999-03-12
K982536 1998-11-24
K941546 1994-09-20
K790975 1979-07-30
K790342 1979-03-22

Recalls Naming This Product

8 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Somatom Emotion 16 Slice (DE)
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Siemens Medical Solutions USA, Inc. 510(k) number 2018-02-15 Class II Software design to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms. Depending on the geometrical shape of the skull bone, 1301 2020-04-08
Siemens Medical Solutions USA, Inc. 510(k) number 2018-02-15 Class II Software design to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms. Depending on the geometrical shape of the skull bone, 1301 2020-04-08
Siemens Medical Solutions USA, Inc. 510(k) number 2018-02-15 Class II Software design to inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms. Depending on the geometrical shape of the skull bone, 1301 2020-04-08
Siemens Medical Solutions USA, Inc. 510(k) number 2018-02-15 Class II Software design To inform customers of possible incorrect tube current calculations by the CARE Dose4D algorithm for head scans based on p.a. (posterior-anterior) or a.p. (anterior-posterior) topograms. Depending on the geometrical shape of the skull bone, 1301 2020-04-08
Siemens Medical Solutions USA, Inc. 510(k) number 2016-02-15 Class II Device Design Siemens is initiating this recall due to a potential malfunction and hence potential hazard to patients and personnel when using the SOMATOM Emotion or SOMATOM Sensation systems in conjunction with the use of the cardio licenses “Cardio Pro 124 units 2016-12-07
Siemens Medical Solutions USA, Inc. 510(k) number 2014-03-21 Class II Component design/selection The rubber damper may degrade and break, causing loosening of the motor mounting plates, which could lead to a series of events that could place the operator and patient at risk of injury. 345 2015-03-16
Siemens Medical Solutions USA, Inc. 510(k) number 2008-08-05 Not classified Nonconforming Material/Component Potential electrical shock hazard. The LCB power Switch (S1) could break causing the protective plastic cap to come off exposing the energized electrical contacts within the switch. The LCB S1 does have an inline fuse which is designed to o 53 units 2008-11-07
Siemens Medical Solutions USA, Inc. 510(k) number 2006-03-09 Not classified Other When using the LungCare feature in the SOMATOM CT Systems some marks made on CT images may not be saved. 5 units 2006-07-19

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