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SLAx/13-6 MHz

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P24523-01Model TRANSDUCER, SLAX/13-6 MHZ

by Fujifilm Sonosite, Inc.

Identity

Trade Name
SLAx/13-6 MHz EUDAMEDFDA UDI
Generic Name
Surgical ultrasound imaging transducer FDA UDI
Device Name
TRANSDUCER, SLAX/13-6 MHZ EUDAMED
Diagnostic ultrasound transducer FDA UDI
Model / Reference
TRANSDUCER, SLAX/13-6 MHZ EUDAMED
P24523-01 EUDAMEDFDA UDI
Description
Diagnostic ultrasound transducer FDA UDI

Identifiers

Catalog Number
P24523 FDA UDI
Primary DI / UDI-DI
00841517107949 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517107949 EUDAMED
510(k) Number
K130173 FDA UDI
K133454 FDA UDI
K183235 FDA UDI
FDA Product Code
ITX FDA UDI
EMDN Code
Z110402010101 TWO–DIMENSIONAL LINEAR–ARRAY TRANSCUTANEOUS ULTRASOUND PROBES EUDAMED
GMDN Term
Surgical ultrasound imaging transducer FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Extracorporeal ultrasound imaging transducer, hand-held

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

Similar devices

Also classified as Extracorporeal ultrasound imaging transducer, hand-held.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000001075
Authorised Representative
Fujifilm Sonosite B.V. NL-AR-000000046

Sources (2)

  • EUDAMED 9d162118-2a66-439e-8fda-51e9550ab11f 61 fields · synced Jul 9, 2026
  • FDA UDI 932300b6-4c91-46ff-bdf0-b0daea4f1d6c 36 fields · synced May 30, 2026