E-ST Pro

FDA UDI

Class II (US FDA UDI)

by Avante

Identity

Trade Name: E-ST Pro FDA UDI
Generic Name: General-purpose ultrasound imaging system FDA UDI
Model / Reference: 60132PRO8 FDA UDI

Identifiers

Primary DI / UDI-DI: 00815871021494 FDA UDI
FDA Product Code: HEP FDA UDI
KNG FDA UDI
GMDN Term: General-purpose ultrasound imaging system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.2660 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

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

E-ST Pro by Avante — 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: Avante

Sources (1)

FDA UDI c5a24ba1-5c0a-4d3c-9772-89b983267ba4 33 fields · synced Jun 1, 2026