gudid
Primary ID: MaxVenturi Acrylic
Flowmeter (UDI MaxVenturi Acrylic)
Manufactured by MAXTEC, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flowmeter - Primary ID MaxVenturi Acrylic
Device Regulatory Overview
The Flowmeter (Model/Catalog Number: MaxVenturi 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
- MaxVenturi Acrylic
- Product Code / EMDN
- BXY
- Device Name
- Flowmeter, MaxVenturi Acrylic
- Database Sync Date
- 2026-08-09 09:32:57
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Flowmeter?
The registered manufacturer of record for Flowmeter is MAXTEC, LLC.
What is the Primary UDI-DI identifier for Flowmeter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MaxVenturi 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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint