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VuMAX

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref BU.575Model VuMAX BU

by Sonomed, Inc.

Identity

Trade Name
VuMAX EUDAMED
VuMAX HD Ophthalmic Ultrasound System FDA UDI
Generic Name
Ophthalmic ultrasound imaging system FDA UDI
Device Name
VuMAX Ophthalmic Ultrasound EUDAMED
The VuMAX HD Ophthalmic Ultrasound System is a non-invasive, active, bio-microscope (UBM) device for imaging ocular features for diagnostic purposes.The B-scan modes ultilizes a sealed 12 MHz B-probe with a focused transducer and a water path probe with 35 MHz and/or 50 MHz transducer. Th system operates on a computer-based platform. B-scan settings include orbit, virtreous body, retina surface, and deep retina/choroid. UBM capabilities include sulcus-to-sulcus, angle detail, high resolution, and motion picture settings. The system includes the multi-frequency ultrasound system base unit, 22" LCD, water-path probe with 35 MHz transducer, 12 MHz B-probe, keyboard and mouse, USB foot switch, immersion cups and user manual. FDA UDI
Model / Reference
VuMAX BU EUDAMED
BU.575 EUDAMED
VuMAX HD B/UBM FDA UDI
Description
The VuMAX HD Ophthalmic Ultrasound System is a non-invasive, active, bio-microscope (UBM) device for imaging ocular features for diagnostic purposes.The B-scan modes ultilizes a sealed 12 MHz B-probe with a focused transducer and a water path probe with 35 MHz and/or 50 MHz transducer. Th system operates on a computer-based platform. B-scan settings include orbit, virtreous body, retina surface, and deep retina/choroid. UBM capabilities include sulcus-to-sulcus, angle detail, high resolution, and motion picture settings. The system includes the multi-frequency ultrasound system base unit, 22" LCD, water-path probe with 35 MHz transducer, 12 MHz B-probe, keyboard and mouse, USB foot switch, immersion cups and user manual. FDA UDI

Identifiers

Catalog Number
BU.575 FDA UDI
Primary DI / UDI-DI
00896100002224 EUDAMEDFDA UDI
Basic UDI-DI
B-00896100002224 EUDAMED
510(k) Number
K060626 FDA UDI
FDA Product Code
IYO FDA UDI
EMDN Code
Z11040199 ULTRASOUND SCANNERS - OTHER EUDAMED
GMDN Term
Ophthalmic ultrasound imaging system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
Market of Registration
Italy 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

VuMAX by Sonomed, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sonomed, Inc.
EUDAMED SRN
US-MF-000002342
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED c8b51dc0-acdb-4c03-8f53-0fc84da87ca6 61 fields · synced Jul 22, 2026
  • FDA UDI f29cc1ce-9602-4b15-b574-ed3e7ab097ec 36 fields · synced May 25, 2026