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P22

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref /Model P20

by Sonoscape Medical Corp.

Identity

Trade Name
P22 EUDAMED
Sonoscape FDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
Digital Color Doppler Ultrasound System EUDAMED
P22 Digital Color Doppler Ultrasound System FDA UDI
Model / Reference
P20 EUDAMED
/ EUDAMED
P22 FDA UDI
Description
P22 Digital Color Doppler Ultrasound System FDA UDI

Identifiers

Primary DI / UDI-DI
06945868612054 EUDAMEDFDA UDI
Basic UDI-DI
69458686U1011SC EUDAMED
510(k) Number
K172993 FDA UDI
FDA Product Code
IYN FDA UDI
IYO FDA UDI
ITX FDA UDI
EMDN Code
Z11040104 MULTIDISCIPLINARY ULTRASOUND SCANNERS (INTERNAL AND CARDIOLOGY, ETC.) EUDAMED
GMDN Term
General-purpose ultrasound imaging system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1550 FDA UDI
892.1560 FDA UDI
892.1570 FDA UDI
Market of Registration
Netherlands 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

No

FDA UDI

P22 by Sonoscape Medical Corp. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000009623
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED c87d5d28-91d6-4a56-ab39-c5118a3d83e7 61 fields · synced Oct 6, 2026
  • FDA UDI 76afb79d-7411-4955-879f-8b09c9a3c393 34 fields · synced May 30, 2026