Somatom Go.all

Catalogue number 11061638, listed by Siemens Shanghai, Medical Equipment Ltd., China, 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

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 go.All
Listed by Siemens Shanghai, Medical Equipment Ltd., China
FDA product code JAK
Device type System, X-Ray, Tomography, Computed
Device class Class 2
Regulation 21 CFR 892.1750
Establishment Contract manufacturer, Complaint-file establishment, Manufacturer
510(k) K173632
Record published 2018-05-26
Record revised 2025-11-27 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number
Storage Storage environment temperature -20 to 50 °C; Handling environment temperature -20 to 50 °C

Catalogue Numbers

Catalogue numbers for Somatom go.All
Catalogue number Size Status
11061638 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

Recalls Naming This Product

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

Recalls naming the identifiers of Somatom go.All
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Siemens Medical Solutions USA, Inc. 510(k) number 2022-03-07 Class II Software design Software error may result in sporadic problems causing scanning workflow interruptions, unexpected user notifications and image artifacts. Sporadic software errors may also occur during interventional workflows.
Results in potential patient
547 units US
Siemens Medical Solutions USA, Inc. 510(k) number 2021-03-03 Class II Software design SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a, may result in sporadic problems causing scanning workflow interruptions and unexpected user notifications. Delay in diagnosis or patient rescan may occur. S 190 units US 2023-12-28
Siemens Medical Solutions USA, Inc. 510(k) number 2019-09-24 Class II Software design SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT VA20A_SP2 and
active Guide&GO license No dose documentation and no Dose Alert for the special mode i-
Sequence during interventional procedures
14 US 2024-07-08
Siemens Medical Solutions USA, Inc. 510(k) number 2019-07-31 Class II Nonconforming Material/Component The injector holder could potentially fall off together with the injector and the storage box. 0 2020-12-02
Siemens Medical Solutions USA, Inc. 510(k) number 2019-07-31 Class II Nonconforming Material/Component The injector holder could potentially fall off together with the injector and the storage box. 18 units 2020-12-02
Siemens Medical Solutions USA, Inc. 510(k) number 2019-07-31 Class II Nonconforming Material/Component The injector holder could potentially fall off together with the injector and the storage box. 3 units 2020-12-02
Siemens Medical Solutions USA, Inc. 510(k) number 2019-07-31 Class II Nonconforming Material/Component The injector holder could potentially fall off together with the injector and the storage box. 10 units 2020-12-02
Siemens Medical Solutions USA, Inc. 510(k) number 2019-07-31 Class II Nonconforming Material/Component The injector holder could potentially fall off together with the injector and the storage box. 0 2020-12-02
Siemens Medical Solutions USA, Inc. 510(k) number 2019-07-31 Class II Nonconforming Material/Component The injector holder could potentially fall off together with the injector and the storage box. 12 units 2020-12-02
Siemens Medical Solutions USA, Inc. 510(k) number 2019-07-31 Class II Nonconforming Material/Component The injector holder could potentially fall off together with the injector and the storage box. 0 2020-12-02
Siemens Medical Solutions USA, Inc. 510(k) number 2019-06-04 Class II Software design The potential sporadic performance problems
may cause scanning workflow interruptions and
unexpected user notifications resulting in
diagnostic delay or need for patient rescan.
69 2023-03-29
Siemens Medical Solutions USA, Inc. 510(k) number 2019-06-04 Class II Software design The potential sporadic performance problems
may cause scanning workflow interruptions and
unexpected user notifications resulting in
diagnostic delay or need for patient rescan.
69 2023-03-29
Siemens Medical Solutions USA, Inc. 510(k) number 2019-06-04 Class II Software design The potential sporadic performance problems
may cause scanning workflow interruptions and
unexpected user notifications resulting in
diagnostic delay or need for patient rescan.
69 2023-03-29
Siemens Medical Solutions USA, Inc. 510(k) number 2019-06-04 Class II Software design The potential sporadic performance problems
may cause scanning workflow interruptions and
unexpected user notifications resulting in
diagnostic delay or need for patient rescan.
69 2023-03-29
Siemens Medical Solutions USA, Inc. 510(k) number 2019-05-28 Class II Software design The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user
notifications. This may cause a delay in diagnosis or patient scans.
9 2023-03-31
Siemens Medical Solutions USA, Inc. 510(k) number 2019-05-28 Class II Software design The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user
notifications. This may cause a delay in diagnosis or patient scans.
53 2023-03-31
Siemens Medical Solutions USA, Inc. 510(k) number 2019-05-28 Class II Software design The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user
notifications. This may cause a delay in diagnosis or patient scans.
24 2023-03-31
Siemens Medical Solutions USA, Inc. 510(k) number 2019-05-28 Class II Software design The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user
notifications. This may cause a delay in diagnosis or patient scans.
30 2023-03-31

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