gudid
Primary ID: 6040-EAVS
MIDAS, PORT, 60%-W-O2, EAVS (UDI 6040-EAVS)
Manufactured by PARKER-HANNIFIN CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MIDAS, PORT, 60%-W-O2, EAVS - Primary ID 6040-EAVS
Device Regulatory Overview
The MIDAS, PORT, 60%-W-O2, EAVS (Model/Catalog Number: 6040-EAVS) is a medical device manufactured by PARKER-HANNIFIN CORPORATION. This product is indexed under FDA Product Code / Category Classification BZR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6040-EAVS
- Product Code / EMDN
- BZR
- Device Name
- Midas Flowmeter, Portable, 60% Max, O2 Control+ eAVS
- Database Sync Date
- 2026-08-09 09:31:28
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 MIDAS, PORT, 60%-W-O2, EAVS?
The registered manufacturer of record for MIDAS, PORT, 60%-W-O2, EAVS is PARKER-HANNIFIN CORPORATION.
What is the Primary UDI-DI identifier for MIDAS, PORT, 60%-W-O2, EAVS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6040-EAVS.
What classification code is assigned to this device?
This device is registered under product classification code BZR.
Similar Classification Devices (BZR)
Other Devices by PARKER-HANNIFIN CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint