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P21xp/5-1 MHz

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P14563-20AModel TRANSDUCER, P21XP/5-1 MHZ

by Fujifilm Sonosite, Inc.

Identity

Trade Name
P21xp/5-1 MHz EUDAMEDFDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
TRANSDUCER, P21XP/5-1 MHZ EUDAMED
Diagnostic Ultrasound Transducer FDA UDI
Model / Reference
TRANSDUCER, P21XP/5-1 MHZ EUDAMED
P14563-20A EUDAMEDFDA UDI
Description
Diagnostic Ultrasound Transducer FDA UDI

Identifiers

Primary DI / UDI-DI
00841517101145 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517101145 EUDAMED
510(k) Number
K152209 FDA UDI
FDA Product Code
ITX FDA UDI
EMDN Code
Z110402010301 TRANSCUTANEOUS ULTRASOUND SECTOR PROBES (PHASED ARRAY), 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
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

P21xp/5-1 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

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Manufacturer

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

Sources (2)

  • EUDAMED 3a2d8eeb-8485-4217-9ee3-de8a5bd7a585 61 fields · synced Aug 2, 2026
  • FDA UDI 7e4796c8-96bd-4c51-9afb-438bb724d864 36 fields · synced May 30, 2026