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SLAx/13-6 MHz

FDA UDI

Class II (US FDA UDI)

by Fujifilm Sonosite, Inc.

Identity

Trade Name
SLAx/13-6 MHz FDA UDI
Generic Name
Surgical ultrasound imaging transducer FDA UDI
Device Name
Diagnostic Ultrasound Transducer FDA UDI
Model / Reference
P05174-71 FDA UDI
Description
Diagnostic Ultrasound Transducer FDA UDI

Identifiers

Catalog Number
P05174 FDA UDI
Primary DI / UDI-DI
00841517104092 FDA UDI
510(k) Number
K043559 FDA UDI
K053069 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Surgical ultrasound imaging transducer 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: Surgical ultrasound imaging transducer

SLAx/13-6 MHz by Fujifilm Sonosite, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical ultrasound imaging transducer.

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 82cf0176-7f68-4ae4-acc4-89bc595e5a53 37 fields · synced May 30, 2026