gudid
Primary ID: 602
McKesson (UDI 602)
Manufactured by MCKESSON MEDICAL-SURGICAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for McKesson - Primary ID 602
Device Regulatory Overview
The McKesson (Model/Catalog Number: 602) is a medical device manufactured by MCKESSON MEDICAL-SURGICAL INC.. This product is indexed under FDA Product Code / Category Classification GKG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 602
- Product Code / EMDN
- GKG
- Device Name
- Centrifuge 6 Place Fixed Angle Rotor Variable Speed up to 4,000 RPM
- Database Sync Date
- 2026-08-09 09:59:18
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of McKesson?
The registered manufacturer of record for McKesson is MCKESSON MEDICAL-SURGICAL INC..
What is the Primary UDI-DI identifier for McKesson?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 602.
What classification code is assigned to this device?
This device is registered under product classification code GKG.
Similar Classification Devices (GKG)
Other Devices by MCKESSON MEDICAL-SURGICAL INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint