gudid
Primary ID: MaxO2+
Analyzer (UDI MaxO2+)
Manufactured by MAXTEC, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Analyzer - Primary ID MaxO2+
Device Regulatory Overview
The Analyzer (Model/Catalog Number: MaxO2+) is a medical device manufactured by MAXTEC, LLC. This product is indexed under FDA Product Code / Category Classification CCL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MaxO2+
- Product Code / EMDN
- CCL
- Device Name
- Analyzer, MaxO2+ A with 60 PSI BlenderBuddy
- Database Sync Date
- 2026-08-09 09:32:57
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 Analyzer?
The registered manufacturer of record for Analyzer is MAXTEC, LLC.
What is the Primary UDI-DI identifier for Analyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MaxO2+.
What classification code is assigned to this device?
This device is registered under product classification code CCL.
Similar Classification Devices (CCL)
Other Devices by MAXTEC, LLC
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