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C322

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref -Model 3C-ARef _Ref /

by Sonoscape Medical Corp.

Identity

Trade Name
C322 EUDAMED
SonoScape FDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
Ultrasonic Transducer EUDAMED
C322 Ultrasonic Transducer (X5 Series) FDA UDI
Model / Reference
3C-A EUDAMED
- EUDAMED
_ EUDAMED
/ EUDAMED
C322 FDA UDI
Description
C322 Ultrasonic Transducer (X5 Series) FDA UDI

Identifiers

Primary DI / UDI-DI
06945868607043 EUDAMED
06945868615376 EUDAMED
06945868620899 EUDAMEDFDA UDI
Basic UDI-DI
69458686P1004QQ EUDAMED
Direct Marketing DI
06945868607043 EUDAMED
06945868615376 EUDAMED
06945868620899 EUDAMED
510(k) Number
K182648 FDA UDI
FDA Product Code
ITX FDA UDI
IYO FDA UDI
IYN 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
892.1560 FDA UDI
892.1550 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

C322 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 (4)

  • EUDAMED 4033d766-8a10-444e-b2b8-658f5142caf4 61 fields · synced Oct 6, 2026
  • EUDAMED 2fdd8731-1f50-4b73-bf58-0385f85e272a 61 fields · synced May 17, 2026
  • EUDAMED d732f1ff-f73d-44f8-9305-f8c273ece0bc 61 fields · synced May 19, 2026
  • FDA UDI 354cbb22-dde7-4b7d-b61e-aeb9844dd5b7 34 fields · synced May 30, 2026