gudid
Primary ID: 5436709
CELSITE (UDI 5436709)
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 CELSITE - Primary ID 5436709
Device Regulatory Overview
The CELSITE (Model/Catalog Number: 5436709) 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
- 5436709
- Product Code / EMDN
- LJT
- Device Name
- CELSITE ST311 ST SET SIL 8,5F 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 CELSITE?
The registered manufacturer of record for CELSITE is B BRAUN INTERVENTIONAL SYSTEMS, INC.
What is the Primary UDI-DI identifier for CELSITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5436709.
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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