gudid
Primary ID: High Flow
MaxBlend2 (UDI High Flow)
Manufactured by MAXTEC, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MaxBlend2 - Primary ID High Flow
Device Regulatory Overview
The MaxBlend2 (Model/Catalog Number: High Flow) is a medical device manufactured by MAXTEC, LLC. This product is indexed under FDA Product Code / Category Classification BZR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- High Flow
- Product Code / EMDN
- BZR
- Device Name
- MaxBlend2 High Flow 0-70 LPM Flowmeter DISS Fitting
- 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 MaxBlend2?
The registered manufacturer of record for MaxBlend2 is MAXTEC, LLC.
What is the Primary UDI-DI identifier for MaxBlend2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is High Flow.
What classification code is assigned to this device?
This device is registered under product classification code BZR.
Similar Classification Devices (BZR)
Other Devices by MAXTEC, LLC
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