gudid
Primary ID: 415066
SAFESITE (UDI 415066)
Manufactured by B. BRAUN MEDICAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SAFESITE - Primary ID 415066
Device Regulatory Overview
The SAFESITE (Model/Catalog Number: 415066) 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
- 415066
- Product Code / EMDN
- FPA
- Device Name
- RV1000FC REFLUX VLVEHINGE CAP
- Database Sync Date
- 2026-08-09 09:10:23
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 SAFESITE?
The registered manufacturer of record for SAFESITE is B. BRAUN MEDICAL INC..
What is the Primary UDI-DI identifier for SAFESITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 415066.
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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