syngo.CT Dual Energy

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare

Identity

Trade Name: syngo.CT Dual Energy FDA UDI
Generic Name: CT system application software FDA UDI
Model / Reference: 11546307 FDA UDI

Identifiers

Primary DI / UDI-DI: 04056869267340 FDA UDI
510(k) Number: K212889 FDA UDI
FDA Product Code: JAK FDA UDI
GMDN Term: CT system application software 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: CT system application software

syngo.CT Dual Energy by Siemens Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Siemens Healthcare

Sources (1)

FDA UDI 34a1f74a-9e22-4ab9-9bc1-e5e226fb5e42 34 fields · synced May 30, 2026