gudid
Primary ID: 2012HZ
Ventlab (UDI 2012HZ)
Manufactured by VENTLAB, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ventlab - Primary ID 2012HZ
Device Regulatory Overview
The Ventlab (Model/Catalog Number: 2012HZ) is a medical device manufactured by VENTLAB, LLC. This product is indexed under FDA Product Code / Category Classification NHK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2012HZ
- Product Code / EMDN
- NHK
- Device Name
- 1 L Hyperinflation system w/ manometer & 25cm pop-off
- Database Sync Date
- 2026-08-09 09:28:44
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 Ventlab?
The registered manufacturer of record for Ventlab is VENTLAB, LLC.
What is the Primary UDI-DI identifier for Ventlab?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2012HZ.
What classification code is assigned to this device?
This device is registered under product classification code NHK.
Similar Classification Devices (NHK)
Other Devices by VENTLAB, LLC
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