Arietta 65

FDA UDI

Class II (US FDA UDI)

by FUJIFILM Corporation

Identity

Trade Name: ARIETTA 65 FDA UDI
Generic Name: General-purpose ultrasound imaging system FDA UDI
Device Name: Diagnostic Ultrasound System FDA UDI
Model / Reference: ARIETTA 65 FDA UDI
Description: Diagnostic Ultrasound System FDA UDI

Identifiers

Primary DI / UDI-DI: 04573596213889 FDA UDI
510(k) Number: K181376 FDA UDI
K202422 FDA UDI
FDA Product Code: IYO FDA UDI
IYN FDA UDI
ITX FDA UDI
GMDN Term: General-purpose ultrasound imaging system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1560 FDA UDI
892.1550 FDA UDI
892.1570 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose ultrasound imaging system

Arietta 65 by FUJIFILM Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose ultrasound imaging system.

SE12-3 Gen II® — SUPERSONIC IMAGINE · Class II
SUPERSONIC MACH 40 — SUPERSONIC IMAGINE · Class II
HS50 — SAMSUNG MEDISON CO., LTD · Class II
EBit Series Diagnostic Ultrasound System — CHISON Medical Technologies Co., Ltd. · Class II
Display Module(M5, International, Alone) — Shenzhen Mindray Bio-Medical Electronics Co. · Class II
WS80A Diagnostic Ultrasound System — SAMSUNG MEDISON CO., LTD · Class II
HS50 / HS60 Diagnostic Ultrasound System — SAMSUNG MEDISON CO., LTD · Class II
MEDISONO — Medisono, LLC · Class II

Cleared under the same submission

K181376 also covers:

ARIETTA 650 — FUJIFILM Corporation

K202422 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: FUJIFILM Corporation

Sources (1)

FDA UDI 36703849-612d-4609-8ef8-bf3e6a1533d2 35 fields · synced May 30, 2026