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L752

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref -Model 12L-A

by Sonoscape Medical Corp.

Identity

Trade Name
L752 EUDAMED
SonoScape FDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
Ultrasonic Transducer EUDAMED
L752 Ultrasonic Transducer (S9) FDA UDI
Model / Reference
12L-A EUDAMED
- EUDAMED
L752 FDA UDI
Description
L752 Ultrasonic Transducer (S9) FDA UDI

Identifiers

Primary DI / UDI-DI
06945868600167 EUDAMEDFDA UDI
Basic UDI-DI
69458686P1001QJ EUDAMED
Direct Marketing DI
06945868600167 EUDAMED
510(k) Number
K152165 FDA UDI
FDA Product Code
ITX FDA UDI
IYO FDA UDI
IYN FDA UDI
EMDN Code
Z110402010101 TWO–DIMENSIONAL LINEAR–ARRAY TRANSCUTANEOUS ULTRASOUND PROBES 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

Category: Extracorporeal ultrasound imaging transducer, hand-held

L752 by Sonoscape Medical Corp. — 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
CN-MF-000009623
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED 384eb5c9-faf2-4e8f-b225-e678164ab348 61 fields · synced Jun 17, 2026
  • FDA UDI 000d4b6e-1722-45a3-9be1-41669d5b7479 34 fields · synced May 30, 2026