gudid
Primary ID: 16-0538-B
McKesson (UDI 16-0538-B)
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 16-0538-B
Device Regulatory Overview
The McKesson (Model/Catalog Number: 16-0538-B) is a medical device manufactured by MCKESSON MEDICAL-SURGICAL INC.. This product is indexed under FDA Product Code / Category Classification CCK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 16-0538-B
- Product Code / EMDN
- CCK
- Device Name
- CANNULA, NASAL GAS SAMP 02/CO2ML ADLT 10'
- Database Sync Date
- 2026-08-09 09:31:00
Full Regulatory Attributes
🔒 Token Gated
{
"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?
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 16-0538-B.
What classification code is assigned to this device?
This device is registered under product classification code CCK.
Similar Classification Devices (CCK)
Other Devices by MCKESSON MEDICAL-SURGICAL INC.
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