← Back to catalogue

C60e/5-2 Mhz

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P07633-21AModel TRANSDUCER, C60E/5-2 MHZ

by Fujifilm Sonosite, Inc.

Identity

Trade Name
C60E/5-2 MHZ EUDAMEDFDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
TRANSDUCER, C60E/5-2 MHZ EUDAMED
Model / Reference
TRANSDUCER, C60E/5-2 MHZ EUDAMED
P07633-21A EUDAMEDFDA UDI

Identifiers

Catalog Number
P07633 FDA UDI
Primary DI / UDI-DI
00841517102845 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517102845 EUDAMED
510(k) Number
K053069 FDA UDI
FDA Product Code
ITX FDA UDI
EMDN Code
Z110402010201 CURVILINEAR TRANSCUTANEOUS TWO–DIMENSIONAL ULTRASOUND PROBES (CONVEX–ARRAY) 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

Category: Extracorporeal ultrasound imaging transducer, hand-held

C60e/5-2 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

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 e3ad31c1-c318-41ed-b0f7-5ce1860d57a3 61 fields · synced Jul 9, 2026
  • FDA UDI 80f505c1-c4f8-4a91-8c55-99438cdbf438 36 fields · synced May 30, 2026