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rC60xi/5-2 MHz

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref rC60xi/5-2 MHz ArmoredModel TRANSDUCER, RC60XI/5-2 MHZ

by Fujifilm Sonosite, Inc.

Identity

Trade Name
rC60xi/5-2 MHz EUDAMED
rC60xi/5-2 MHz Armored FDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
TRANSDUCER, RC60XI/5-2 MHZ EUDAMED
Model / Reference
TRANSDUCER, RC60XI/5-2 MHZ EUDAMED
rC60xi/5-2 MHz Armored EUDAMED
P21636-20 FDA UDI

Identifiers

Catalog Number
P21636 FDA UDI
Primary DI / UDI-DI
00841517104917 EUDAMEDFDA UDI
Basic UDI-DI
08415171RC60XI8H EUDAMED
510(k) Number
K162045 FDA UDI
K183235 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

rC60xi/5-2 MHz 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 b596f37a-f6e7-44a2-84d5-b2312fa2dca7 61 fields · synced Jul 13, 2026
  • FDA UDI a6fdfc8b-99ac-49e1-8714-8d3b2b81033d 36 fields · synced May 30, 2026