gudid
Primary ID: 13.2.1
McKesson Cardiology Hemo (UDI 13.2.1)
Manufactured by Change Healthcare Canada Company
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for McKesson Cardiology Hemo - Primary ID 13.2.1
Device Regulatory Overview
The McKesson Cardiology Hemo (Model/Catalog Number: 13.2.1) is a medical device manufactured by Change Healthcare Canada Company. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13.2.1
- Product Code / EMDN
- DQK
- Device Name
- Database Sync Date
- 2026-08-09 09:16:45
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of McKesson Cardiology Hemo?
The registered manufacturer of record for McKesson Cardiology Hemo is Change Healthcare Canada Company.
What is the Primary UDI-DI identifier for McKesson Cardiology Hemo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13.2.1.
What classification code is assigned to this device?
This device is registered under product classification code DQK.
Similar Classification Devices (DQK)
Other Devices by Change Healthcare Canada Company
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