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2-MHz Transducer, Handheld

FDA UDI

Class II (US FDA UDI)

by Novasignal Corporation

Identity

Trade Name
2-MHz Transducer, Handheld FDA UDI
Generic Name
Noninvasive vascular ultrasound system probe FDA UDI
Device Name
The handheld transducer is a 2 MHz single-element ultrasound transducer designed to be held by hand to perform velocity measurements. The transducer has the following specifications: • 2MHz ± 0.1MHz center frequency • 46mm ± 5mm focal length • 16mm active diameter • Fractional 6dB pulse-echo bandwidth = 60% to 80% • Round-trip insertion loss < 6dB • Impedance 22 ohm +/- 5 ohms, real 0°+/- 15° phase FDA UDI
Model / Reference
40-00008 FDA UDI
Description
The handheld transducer is a 2 MHz single-element ultrasound transducer designed to be held by hand to perform velocity measurements. The transducer has the following specifications: • 2MHz ± 0.1MHz center frequency • 46mm ± 5mm focal length • 16mm active diameter • Fractional 6dB pulse-echo bandwidth = 60% to 80% • Round-trip insertion loss < 6dB • Impedance 22 ohm +/- 5 ohms, real 0°+/- 15° phase FDA UDI

Identifiers

Catalog Number
NA – PRB1 FDA UDI
Primary DI / UDI-DI
00850681007016 FDA UDI
510(k) Number
K160442 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Noninvasive vascular ultrasound system probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 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: Noninvasive vascular ultrasound system probe

2-MHz Transducer, Handheld by Novasignal Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive vascular ultrasound system probe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 24893d71-2cfb-403f-b38f-914239bc7558 35 fields · synced May 30, 2026