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Viz HCM

FDA UDI

Class II (US FDA UDI)

by Viz.ai

Identity

Trade Name
Viz HCM FDA UDI
Generic Name
Cardiopulmonary physiological parameter analysis software FDA UDI
Device Name
Viz HCM v1.1 (2024-06-19) FDA UDI
Model / Reference
Viz HCM Software FDA UDI
Description
Viz HCM v1.1 (2024-06-19) FDA UDI

Identifiers

Primary DI / UDI-DI
00811852030332 FDA UDI
510(k) Number
FDA Product Code
QXO FDA UDI
GMDN Term
Cardiopulmonary physiological parameter analysis software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2380 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: Cardiopulmonary physiological parameter analysis software

Viz HCM by Viz.ai — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary physiological parameter analysis software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Viz.ai

Sources (1)

  • FDA UDI 9619ed9e-8888-4cec-8d3b-a0a37ef9ce8e 35 fields · synced Jun 9, 2026