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P30 Exp

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref /Model P50 Exp

by Sonoscape Medical Corp.

Identity

Trade Name
P30 Exp EUDAMED
Sonoscape FDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
Digital Color Doppler Ultrasound System EUDAMED
P30 Exp Series Digital Color Doppler Ultrasound System FDA UDI
Model / Reference
P50 Exp EUDAMED
/ EUDAMED
P30 Exp FDA UDI
Description
P30 Exp Series Digital Color Doppler Ultrasound System FDA UDI

Identifiers

Primary DI / UDI-DI
06945868613044 EUDAMEDFDA UDI
Basic UDI-DI
69458686U1010SA EUDAMED
510(k) Number
K170999 FDA UDI
FDA Product Code
ITX FDA UDI
IYO FDA UDI
IYN 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
892.1570 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

P30 Exp 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 6c418257-ec2e-4959-9932-45fa577bbdd0 61 fields · synced Oct 6, 2026
  • FDA UDI 21b8ed7e-8d77-4c75-a23c-767967faea79 34 fields · synced May 30, 2026