EPIQ 5W Ultrasound System

FDA UDI

Class II (US FDA UDI)

by Philips Ultrasound LLC

Identity

Trade Name: EPIQ 5W Ultrasound System FDA UDI
Generic Name: General-purpose ultrasound imaging system FDA UDI
Model / Reference: 795206 FDA UDI

Identifiers

Primary DI / UDI-DI: 00884838107519 FDA UDI
FDA Product Code: LLZ FDA UDI
IYN FDA UDI
IYO FDA UDI
ITX FDA UDI
OBJ FDA UDI
QIH FDA UDI
GMDN Term: General-purpose ultrasound imaging system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.2050 FDA UDI
892.1550 FDA UDI
892.1560 FDA UDI
892.1570 FDA UDI
870.1200 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

FDA UDI

Category: General-purpose ultrasound imaging system

EPIQ 5W Ultrasound System by Philips Ultrasound LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Philips Ultrasound LLC

Sources (1)

FDA UDI be35db3f-2129-430e-9ee2-00ba1e8722b3 32 fields · synced Jun 8, 2026