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EchoGo

FDA UDI

Class II (US FDA UDI)

by Ultromics, Ltd.

Identity

Trade Name
EchoGo FDA UDI
Generic Name
Radiology DICOM image processing application software FDA UDI
Model / Reference
Core FDA UDI

Identifiers

Primary DI / UDI-DI
05060634690003 FDA UDI
510(k) Number
K191171 FDA UDI
FDA Product Code
QIH FDA UDI
GMDN Term
Radiology DICOM image processing application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiology DICOM image processing application softwareCardiac mapping system application softwareUltrasound imaging system application software

EchoGo by Ultromics, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasound imaging system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ultromics, Ltd.

Sources (1)

  • FDA UDI a1951eeb-e301-410d-a1d4-311d5e1e529b 33 fields · synced Jun 1, 2026