← Back to catalogue

McKesson Cardiology™

FDA UDI

Class II (US FDA UDI)

by Change Healthcare Canada Company

Identity

Trade Name
McKesson Cardiology™ FDA UDI
Generic Name
Cardiology information system FDA UDI
Model / Reference
13.2.1 FDA UDI

Identifiers

Primary DI / UDI-DI
80010939070018 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Cardiology information system 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

No

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: Cardiology information system

McKesson Cardiology™ by Change Healthcare Canada Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiology information system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Change Healthcare Canada Company

Sources (1)

  • FDA UDI 6793dc68-bc85-4870-9659-26fbc899af73 32 fields · synced Jun 6, 2026