gudid
Primary ID: 0-15 LPM Thorpe Carefusion
DFB Flowmeter (UDI 0-15 LPM Thorpe Carefusion)
Manufactured by MAXTEC, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DFB Flowmeter - Primary ID 0-15 LPM Thorpe Carefusion
Device Regulatory Overview
The DFB Flowmeter (Model/Catalog Number: 0-15 LPM Thorpe Carefusion) 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
- 0-15 LPM Thorpe Carefusion
- Product Code / EMDN
- BXY
- Device Name
- DFB Flowmeter, 0-15 LPM Thorpe 60 PSI with DISS Fitting Carefusion
- 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 DFB Flowmeter?
The registered manufacturer of record for DFB Flowmeter is MAXTEC, LLC.
What is the Primary UDI-DI identifier for DFB Flowmeter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0-15 LPM Thorpe Carefusion.
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