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Sonata® System Cart

FDA UDI

Class II (US FDA UDI)

by Gynesonics, Inc.

Identity

Trade Name
Sonata® System Cart FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
Electromechanical device transport trolley FDA UDI
Model / Reference
ACCY-002 FDA UDI
Description
Electromechanical device transport trolley FDA UDI

Identifiers

Catalog Number
ACCY-002 FDA UDI
Primary DI / UDI-DI
10817929020180 FDA UDI
FDA Product Code
IYO FDA UDI
KNF FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
884.4160 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electromechanical device/system transport trolley

Sonata® System Cart by Gynesonics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical device/system transport trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gynesonics, Inc.

Sources (1)

  • FDA UDI d498f372-4fde-4ebc-bc61-b08a584a42b1 36 fields · synced May 30, 2026