gudid
Primary ID: 415110
ULTRASITE (UDI 415110)
Manufactured by B. BRAUN MEDICAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ULTRASITE - Primary ID 415110
Device Regulatory Overview
The ULTRASITE (Model/Catalog Number: 415110) is a medical device manufactured by B. BRAUN MEDICAL INC.. This product is indexed under FDA Product Code / Category Classification FPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 415110
- Product Code / EMDN
- FPA
- Device Name
- ULTRASITE Luer Access Device
- Database Sync Date
- 2026-08-09 09:38:09
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 ULTRASITE?
The registered manufacturer of record for ULTRASITE is B. BRAUN MEDICAL INC..
What is the Primary UDI-DI identifier for ULTRASITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 415110.
What classification code is assigned to this device?
This device is registered under product classification code FPA.
Similar Classification Devices (FPA)
Other Devices by B. BRAUN MEDICAL INC.
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