gudid
Primary ID: 5408
Venti.Plus (UDI 5408)
Manufactured by GaleMed Xiamen Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Venti.Plus - Primary ID 5408
Device Regulatory Overview
The Venti.Plus (Model/Catalog Number: 5408) is a medical device manufactured by GaleMed Xiamen Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NHK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5408
- Product Code / EMDN
- NHK
- Device Name
- 1.0 HYPERINFLATION W/ MANMTR, MASK
- Database Sync Date
- 2026-08-09 09:15:32
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 Venti.Plus?
The registered manufacturer of record for Venti.Plus is GaleMed Xiamen Co., Ltd..
What is the Primary UDI-DI identifier for Venti.Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5408.
What classification code is assigned to this device?
This device is registered under product classification code NHK.
Similar Classification Devices (NHK)
Other Devices by GaleMed Xiamen Co., Ltd.
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