← Back to catalogue

SonoSite M-Turbo

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P08189-92Model M-TURBO ULTRASOUND SYSTEM, NA

by Fujifilm Sonosite, Inc.

Identity

Trade Name
SonoSite M-Turbo EUDAMEDFDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
M-TURBO ULTRASOUND SYSTEM, NA EUDAMED
M-TURBO ULTRASOUND SYSTEM, 3.0 FDA UDI
Model / Reference
M-TURBO ULTRASOUND SYSTEM, NA EUDAMED
P08189-92 EUDAMEDFDA UDI
Description
M-TURBO ULTRASOUND SYSTEM, 3.0 FDA UDI

Identifiers

Primary DI / UDI-DI
00841517107833 EUDAMEDFDA UDI
Basic UDI-DI
B-00841517107833 EUDAMED
510(k) Number
K071134 FDA UDI
K082098 FDA UDI
K101757 FDA UDI
K130173 FDA UDI
FDA Product Code
ITX FDA UDI
IYN FDA UDI
IYO FDA UDI
OIJ FDA UDI
EMDN Code
Z11040103 PORTABLE ULTRASOUND SCANNERS 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
892.1550 FDA UDI
892.1560 FDA UDI
Market of Registration
Finland 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

SonoSite M-Turbo by Fujifilm Sonosite, 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

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

Manufacturer

EUDAMED SRN
US-MF-000001075
Authorised Representative
Fujifilm Sonosite B.V. NL-AR-000000046

Sources (2)

  • EUDAMED 1284ac2d-2e41-41ac-8529-d4444c303389 61 fields · synced Jun 19, 2026
  • FDA UDI 91223481-412c-4365-95c1-75cd3778133b 35 fields · synced May 30, 2026