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C8x/8-5 MHz

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P24319-02Model TRANSDUCER, C8X/8-5 MHZ CURVED ARRAY, COAX CABLE

by Fujifilm Sonosite, Inc.

Identity

Trade Name
C8x/8-5 MHz EUDAMEDFDA UDI
Generic Name
Rectal/vaginal ultrasound imaging transducer FDA UDI
Device Name
TRANSDUCER, C8X/8-5 MHZ CURVED ARRAY, COAX CABLE EUDAMED
Diagnostic Ultrasound Transducer FDA UDI
Model / Reference
TRANSDUCER, C8X/8-5 MHZ CURVED ARRAY, COAX CABLE EUDAMED
P24319-02 EUDAMEDFDA UDI
Description
Diagnostic Ultrasound Transducer FDA UDI

Identifiers

Primary DI / UDI-DI
00841517106973 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517106973 EUDAMED
FDA Product Code
ITX FDA UDI
IYN FDA UDI
IYO FDA UDI
EMDN Code
Z110402010201 CURVILINEAR TRANSCUTANEOUS TWO–DIMENSIONAL ULTRASOUND PROBES (CONVEX–ARRAY) EUDAMED
GMDN Term
Rectal/vaginal ultrasound imaging transducer 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
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

C8x/8-5 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 863cfe33-2c11-42af-95b2-449acb3c7826 61 fields · synced Jun 19, 2026
  • FDA UDI 3e19f6a1-4654-4d17-aaa7-6c9bf1d9131c 34 fields · synced May 30, 2026