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L38v/10-5 MHz

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P19360-18AModel TRANSDUCER, L38V 10-5 MHZ, IVIZ

by Fujifilm Sonosite, Inc.

Identity

Trade Name
L38v/10-5 MHz EUDAMEDFDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
TRANSDUCER, L38V 10-5 MHZ, IVIZ EUDAMED
Diagnostic Ultrasound Transducer FDA UDI
Model / Reference
TRANSDUCER, L38V 10-5 MHZ, IVIZ EUDAMED
P19360-18A EUDAMEDFDA UDI
Description
Diagnostic Ultrasound Transducer FDA UDI

Identifiers

Catalog Number
P19360 FDA UDI
Primary DI / UDI-DI
00841517102005 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517102005 EUDAMED
FDA Product Code
ITX FDA UDI
EMDN Code
Z1104020201 ENDOCAVITARY ULTRASOUND PROBES, TWO–DIMENSIONAL 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
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

L38v/10-5 MHz by Fujifilm Sonosite, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 38765b35-4b96-4620-926d-b9cd767ba1e3 61 fields · synced May 30, 2026
  • FDA UDI 028f4ca1-217d-4586-ac81-2db2e6e4bc84 36 fields · synced May 30, 2026