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SOMATOM go.Up

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name
SOMATOM go.Up FDA UDI
Generic Name
Full-body CT system FDA UDI
Model / Reference
11061620 FDA UDI

Identifiers

Primary DI / UDI-DI
04056869051314 FDA UDI
510(k) Number
K163296 FDA UDI
K211373 FDA UDI
K233650 FDA UDI
K250822 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Full-body CT system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Full-body CT system

SOMATOM go.Up by Siemens Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Full-body CT system.

Cleared under the same submission

K163296 also covers:

K211373 also covers:

K233650 also covers:

K250822 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare

Sources (1)

  • FDA UDI 50e3bc1c-9c95-4666-a654-ef5f948d489f 35 fields · synced May 30, 2026