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Pr59

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref PR59Model CURVILINEAR TRANSCUTANEOUS ULTRASOUND PROBES (CONVEX-ARRAY)

by Sonoscanner

Identity

Trade Name
PR59 EUDAMED
T-Lite FDA UDI
Generic Name
Extracorporeal ultrasound imaging transducer, hand-held FDA UDI
Device Name
Single Crystal Convex Probe 1.5-6Mhz FDA UDI
Model / Reference
CURVILINEAR TRANSCUTANEOUS ULTRASOUND PROBES (CONVEX-ARRAY) EUDAMED
PR59 EUDAMEDFDA UDI
Description
Single Crystal Convex Probe 1.5-6Mhz FDA UDI

Identifiers

Primary DI / UDI-DI
03701104600154 EUDAMEDFDA UDI
Basic UDI-DI
37011046CAUSPROBESNS EUDAMED
Direct Marketing DI
03701104600154 EUDAMED
510(k) Number
K201988 FDA UDI
FDA Product Code
ITX 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
Market of Registration
France 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

Category: Extracorporeal ultrasound imaging transducer, hand-held

Pr59 by Sonoscanner — 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

Manufacturer
Sonoscanner
EUDAMED SRN
FR-MF-000002220

Sources (2)

  • EUDAMED c9cc3019-d0e9-413c-bc8c-6a4557452527 61 fields · synced Oct 6, 2026
  • FDA UDI 31c4b0e6-e777-4f5f-bb74-5a6cdbc7e643 34 fields · synced May 29, 2026