eudamed_udi
Primary ID: 04046955058495
Perifix® LOR (UDI 04046955058495)
Manufactured by B. Braun Melsungen AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perifix® LOR - Primary ID 04046955058495
Device Regulatory Overview
The Perifix® LOR (Model/Catalog Number: 4638110) is a medical device manufactured by B. Braun Melsungen AG. This product is indexed under FDA Product Code / Category Classification A020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4638110
- Product Code / EMDN
- A020101
- Device Name
- Perifix LOR Syringe
- Database Sync Date
- 2026-08-09 18:29:47
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 Perifix® LOR?
The registered manufacturer of record for Perifix® LOR is B. Braun Melsungen AG.
What is the Primary UDI-DI identifier for Perifix® LOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046955058495.
What classification code is assigned to this device?
This device is registered under product classification code A020101.
Similar Classification Devices (A020101)
Other Devices by B. Braun Melsungen AG
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