gudid
Primary ID: 5430144
B.BRAUN (UDI 5430144)
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 B.BRAUN - Primary ID 5430144
Device Regulatory Overview
The B.BRAUN (Model/Catalog Number: 5430144) is a medical device manufactured by B BRAUN INTERVENTIONAL SYSTEMS, INC. This product is indexed under FDA Product Code / Category Classification LJT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5430144
- Product Code / EMDN
- LJT
- Device Name
- CELSITE STL201L ST SET SIL 8,5F L IV USA
- Database Sync Date
- 2026-08-09 09:43:15
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 B.BRAUN?
The registered manufacturer of record for B.BRAUN is B BRAUN INTERVENTIONAL SYSTEMS, INC.
What is the Primary UDI-DI identifier for B.BRAUN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5430144.
What classification code is assigned to this device?
This device is registered under product classification code LJT.
Similar Classification Devices (LJT)
Other Devices by B BRAUN INTERVENTIONAL SYSTEMS, INC
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