gudid Primary ID: 900-502MCK

McKesson (UDI 900-502MCK)

Manufactured by MCKESSON MEDICAL-SURGICAL INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The McKesson (Model/Catalog Number: 900-502MCK) is a medical device manufactured by MCKESSON MEDICAL-SURGICAL INC.. This product is indexed under FDA Product Code / Category Classification GGM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 900-502MCK
Product Code / EMDN: GGM
Device Name: Control Solution MEDIUM LEVEL
Database Sync Date: 2026-08-09 09:58:18

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 900-502MCK.

What classification code is assigned to this device?

This device is registered under product classification code GGM.

Similar Classification Devices (GGM)

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