gudid
Primary ID: 092946-003
NEUROVENT-P (UDI 092946-003)
Manufactured by RAUMEDIC AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NEUROVENT-P - Primary ID 092946-003
Device Regulatory Overview
The NEUROVENT-P (Model/Catalog Number: 092946-003) is a medical device manufactured by RAUMEDIC AG. This product is indexed under FDA Product Code / Category Classification GWM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 092946-003
- Product Code / EMDN
- GWM
- Device Name
- Database Sync Date
- 2026-08-09 09:11:51
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 NEUROVENT-P?
The registered manufacturer of record for NEUROVENT-P is RAUMEDIC AG.
What is the Primary UDI-DI identifier for NEUROVENT-P?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 092946-003.
What classification code is assigned to this device?
This device is registered under product classification code GWM.
Similar Classification Devices (GWM)
Other Devices by RAUMEDIC AG
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