gudid
Primary ID: 5010028
VENA TECH (UDI 5010028)
Manufactured by B BRAUN INTERVENTIONAL SYSTEMS, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VENA TECH - Primary ID 5010028
Device Regulatory Overview
The VENA TECH (Model/Catalog Number: 5010028) is a medical device manufactured by B BRAUN INTERVENTIONAL SYSTEMS, INC. This product is indexed under FDA Product Code / Category Classification DTK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5010028
- Product Code / EMDN
- DTK
- Device Name
- VenaTech Convertible
- Database Sync Date
- 2026-08-09 09:38:01
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 VENA TECH?
The registered manufacturer of record for VENA TECH is B BRAUN INTERVENTIONAL SYSTEMS, INC.
What is the Primary UDI-DI identifier for VENA TECH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5010028.
What classification code is assigned to this device?
This device is registered under product classification code DTK.
Similar Classification Devices (DTK)
Other Devices by B BRAUN INTERVENTIONAL SYSTEMS, INC
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