gudid
Primary ID: 473989
Filterflow (UDI 473989)
Manufactured by B. BRAUN MEDICAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Filterflow - Primary ID 473989
Device Regulatory Overview
The Filterflow (Model/Catalog Number: 473989) 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
- 473989
- Product Code / EMDN
- FPA
- Device Name
- 0.2 Micron Filtered Extension Set with 1 Non-needle free injection site
- 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 Filterflow?
The registered manufacturer of record for Filterflow is B. BRAUN MEDICAL INC..
What is the Primary UDI-DI identifier for Filterflow?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 473989.
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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