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Focalist System Software

FDA UDI

Class II (US FDA UDI)

by Mendaera, Inc.

Identity

Trade Name
Focalist System Software FDA UDI
Generic Name
Ultrasound imaging system operation software FDA UDI
Model / Reference
rc25 FDA UDI

Identifiers

Primary DI / UDI-DI
00850062065031 FDA UDI
510(k) Number
K250524 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Ultrasound imaging system operation software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 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

No

FDA UDI

Category: Ultrasound imaging system operation software

Focalist System Software by Mendaera, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasound imaging system operation software.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mendaera, Inc.

Sources (1)

  • FDA UDI 1d0c8caf-cec9-4729-95c1-aa19c337b54e 34 fields · synced May 30, 2026