Medisono

FDA UDI

Class II (US FDA UDI)

by Medisono, LLC

Identity

Trade Name: MEDISONO FDA UDI
Generic Name: General-purpose ultrasound imaging system FDA UDI
Device Name: Probe FDA UDI
Model / Reference: PENCIL PROBE MODEL PB-CWD 2.0 FOR MEDISONO MS12 FDA UDI
Description: Probe FDA UDI

Identifiers

Primary DI / UDI-DI: B369MUS05253 FDA UDI
FDA Product Code: IYN FDA UDI
GMDN Term: General-purpose ultrasound imaging system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1550 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

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

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: General-purpose ultrasound imaging system

Medisono by Medisono, LLC — 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: Medisono, LLC

Sources (1)

FDA UDI 4f6a2de0-fed8-4780-895b-c64d9bf2586d 34 fields · synced May 31, 2026