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Arietta 70

FDA UDI

Class II (US FDA UDI)

by FUJIFILM Corporation

Identity

Trade Name
ARIETTA 70 FDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
Diagnostic Ultrasound System FDA UDI
Model / Reference
ARIETTA 70 FDA UDI
Description
Diagnostic Ultrasound System FDA UDI

Identifiers

Primary DI / UDI-DI
04573596213995 FDA UDI
510(k) Number
K134016 FDA UDI
FDA Product Code
IYO FDA UDI
ITX FDA UDI
IYN FDA UDI
GMDN Term
General-purpose ultrasound imaging system FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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: General-purpose ultrasound imaging system

Arietta 70 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8b637412-b856-437d-88e1-344c74dd1770 35 fields · synced Jun 1, 2026