ACUSON Sequoia Select Diagnostic Ultrasound System

FDA UDI

Class II (US FDA UDI)

by Siemens Medical Solutions Usa, Inc.

Identity

Trade Name: ACUSON Sequoia Select Diagnostic Ultrasound System FDA UDI
Generic Name: General-purpose ultrasound imaging system FDA UDI
Model / Reference: 11658635 FDA UDI

Identifiers

Primary DI / UDI-DI: 04056869981062 FDA UDI
510(k) Number: K223735 FDA UDI
K232145 FDA UDI
K240704 FDA UDI
K242523 FDA UDI
FDA Product Code: ITX FDA UDI
IYO FDA UDI
IYN FDA UDI
QIH FDA UDI
GMDN Term: General-purpose ultrasound imaging system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1570 FDA UDI
892.1560 FDA UDI
892.1550 FDA UDI
892.2050 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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: General-purpose ultrasound imaging system

ACUSON Sequoia Select Diagnostic Ultrasound System by Siemens Medical Solutions Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID

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Cleared under the same submission

K232145 also covers:

K240704 also covers:

K242523 also covers:

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 Medical Solutions Usa, Inc.

Sources (1)

FDA UDI ab739332-17b4-4d8f-a547-77b0da26f5a4 35 fields · synced Jun 8, 2026