ASCEND Catalyst Live

FDA UDI

Class I (US FDA UDI)

by Ascend Cardiovascular Llc

Identity

Trade Name: ASCEND Catalyst Live FDA UDI
Generic Name: Video consultation telemedicine system FDA UDI
Device Name: Catalyst Live is a telepresence solution that enables collaboration in imaging, surgical, remote, and hybrid environments. FDA UDI
Model / Reference: 7.2 FDA UDI
Description: Catalyst Live is a telepresence solution that enables collaboration in imaging, surgical, remote, and hybrid environments. FDA UDI

Identifiers

Primary DI / UDI-DI: 00860006348007 FDA UDI
FDA Product Code: OUG FDA UDI
GMDN Term: Video consultation telemedicine system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6310 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

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Video consultation telemedicine system

ASCEND Catalyst Live by Ascend Cardiovascular Llc — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Ascend Cardiovascular Llc

Sources (1)

FDA UDI 5930d07f-7fa8-41f0-b2df-3bd16c5bbe50 34 fields · synced Jun 8, 2026