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L15-4

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P23120-20Model TRANSDUCER, L15-4

by Fujifilm Sonosite, Inc.

Identity

Trade Name
L15-4 EUDAMEDFDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
TRANSDUCER, L15-4 EUDAMEDFDA UDI
Model / Reference
TRANSDUCER, L15-4 EUDAMED
P23120-20 EUDAMEDFDA UDI
Description
TRANSDUCER, L15-4 FDA UDI

Identifiers

Catalog Number
P23120 FDA UDI
Primary DI / UDI-DI
00841517105884 EUDAMEDFDA UDI
Basic UDI-DI
08415171L154BW EUDAMED
510(k) Number
K200964 FDA UDI
FDA Product Code
ITX FDA UDI
IYN FDA UDI
IYO FDA UDI
OIJ FDA UDI
EMDN Code
Z110402010101 TWO–DIMENSIONAL LINEAR–ARRAY TRANSCUTANEOUS ULTRASOUND PROBES EUDAMED
GMDN Term
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
892.1550 FDA UDI
892.1560 FDA UDI
Market of Registration
Denmark EUDAMED
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

L15-4 by Fujifilm Sonosite, Inc. — Class IIa — MDR, 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/MDR

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 670713b4-e5d0-4f82-a71e-3098fd38f6e0 61 fields · synced Jun 19, 2026
  • FDA UDI 699e08aa-0074-4551-b527-7bf945a7a7fe 36 fields · synced May 30, 2026