gudid
Primary ID: 6180-EAVS
MIDAS, REM, 70%-W-N20 , EAVS (UDI 6180-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, REM, 70%-W-N20 , EAVS - Primary ID 6180-EAVS
Device Regulatory Overview
The MIDAS, REM, 70%-W-N20 , EAVS (Model/Catalog Number: 6180-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
- 6180-EAVS
- Product Code / EMDN
- BZR
- Device Name
- Midas Flowmeter, Remote, 70% Max, N2O 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
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MIDAS, REM, 70%-W-N20 , EAVS?
The registered manufacturer of record for MIDAS, REM, 70%-W-N20 , EAVS is PARKER-HANNIFIN CORPORATION.
What is the Primary UDI-DI identifier for MIDAS, REM, 70%-W-N20 , EAVS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6180-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
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