← Back to catalogue

Voluson Expert 18, Voluson Expert 20, Voluson Expert 22

EUDAMEDFDA UDIFDA 510(k)

Class IIa (EU MDR)

Ref Voluson Expert 20 BT24510(k) K242168Ref Voluson Expert 18 BT24

by GE Healthcare Austria GmbH & Co OG

Identity

Trade Name
Voluson Expert 18 BT24 EUDAMED
Voluson FDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
Voluson Expert 18, Voluson Expert 20, Voluson Expert 22 EUDAMED
Voluson Expert 20 BT24 FDA UDI
Voluson Expert 18 BT24 FDA UDI
Model / Reference
Voluson Expert 20 BT24 EUDAMED
Voluson Expert 18 BT24 EUDAMED
Expert 20 BT24 FDA UDI
Expert 18 BT24 FDA UDI
Description
Voluson Expert 20 BT24 FDA UDI
Voluson Expert 18 BT24 FDA UDI

Identifiers

Catalog Number
5934553 FDA UDI
5934554 FDA UDI
Primary DI / UDI-DI
00195278699824 EUDAMEDFDA UDI
00195278699800 EUDAMEDFDA UDI
Basic UDI-DI
8406821BUG00372HL EUDAMED
Direct Marketing DI
00195278699824 EUDAMED
00195278699800 EUDAMED
510(k) Number
K220358 FDA UDI
K231965 FDA UDI
FDA Product Code
IYN FDA UDI
ITX FDA UDI
IYO 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
892.1550 FDA UDI
892.1570 FDA UDI
892.1560 FDA UDI
Market of Registration
Austria 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Voluson Expert 18, Voluson Expert 20, Voluson Expert 22 by GE Healthcare Austria GmbH & Co OG — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA…

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

United States Active

FDA_510K

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
AT-MF-000001461
FDA Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics

Sources (7)

  • EUDAMED d5323171-0871-4cf0-b5cf-b06f0a063928 85 fields · synced Oct 7, 2026
  • EUDAMED a28d6928-2914-4256-beec-36e6eb296ec3 61 fields · synced May 17, 2026
  • FDA UDI 9c94a4a8-0f1b-4045-8d74-bfd6a5e87904 37 fields · synced May 29, 2026
  • FDA UDI f3bae188-62ae-469d-8024-01c99c9e7d09 37 fields · synced May 30, 2026
  • EUDAMED 2ab0f131-f053-4182-93d7-04d0fa432ebd 61 fields · synced Jun 18, 2026
  • EUDAMED 32625177-a796-4d49-8171-af97d6b44e07 61 fields · synced Jul 22, 2026
  • FDA 510(k) K242168 1 fields · synced May 18, 2026