gudid
Primary ID: 0-30 LPM Acrylic
Manifold (UDI 0-30 LPM Acrylic)
Manufactured by MAXTEC, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Manifold - Primary ID 0-30 LPM Acrylic
Device Regulatory Overview
The Manifold (Model/Catalog Number: 0-30 LPM Acrylic) is a medical device manufactured by MAXTEC, LLC. This product is indexed under FDA Product Code / Category Classification BXY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0-30 LPM Acrylic
- Product Code / EMDN
- BXY
- Device Name
- Manifold, 0-30 LPM Acrylic Flowmeter with 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 Manifold?
The registered manufacturer of record for Manifold is MAXTEC, LLC.
What is the Primary UDI-DI identifier for Manifold?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0-30 LPM Acrylic.
What classification code is assigned to this device?
This device is registered under product classification code BXY.
Similar Classification Devices (BXY)
Other Devices by MAXTEC, LLC
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