gudid Primary ID: 181-35225

McKesson (UDI 181-35225)

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: 181-35225) is a medical device manufactured by MCKESSON MEDICAL-SURGICAL INC.. This product is indexed under FDA Product Code / Category Classification DHA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 181-35225
Product Code / EMDN: DHA
Device Name: HCG Dipsticks
Database Sync Date: 2026-08-09 09:58:18

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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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 181-35225.

What classification code is assigned to this device?

This device is registered under product classification code DHA.

Similar Classification Devices (DHA)

Other Devices by MCKESSON MEDICAL-SURGICAL INC.

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