gudid
Primary ID: HS4051-O
Ventlab (UDI HS4051-O)
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 HS4051-O
Device Regulatory Overview
The Ventlab (Model/Catalog Number: HS4051-O) 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
- HS4051-O
- Product Code / EMDN
- NHK
- Device Name
- .5 LITRE HYPERINFLATION BAG SYSTEM W/ MANOMETER W/O'RING
- Database Sync Date
- 2026-08-09 09:28:45
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 HS4051-O.
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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