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Sonosite ST Stand

FDA UDIEUDAMED

Class II (US FDA UDI)

by Fujifilm Sonosite, Inc.

Identity

Trade Name
Sonosite ST Stand FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
Sonosite ST Stand FDA UDI
Model / Reference
P31204-20 FDA UDI
Description
Sonosite ST Stand FDA UDI

Identifiers

Catalog Number
P31204 FDA UDI
Primary DI / UDI-DI
00841517109226 FDA UDI
510(k) Number
K213763 FDA UDI
FDA Product Code
ITX FDA UDI
IYN FDA UDI
IYO FDA UDI
OIJ FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

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

Yes

FDA UDI

Category: Electromechanical device/system transport trolley

Sonosite ST Stand by Fujifilm Sonosite, Inc. — Class II — MDD, MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical device/system transport trolley.

Cleared under the same submission

K213763 also covers:

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fujifilm Sonosite, Inc.

Sources (2)

  • FDA UDI 5a2ee69b-7174-4056-a724-64024a8ccef6 36 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026