eudamed_udi
Primary ID: 08052747955329
KARL-DEFLUX (UDI 08052747955329)
Manufactured by PHOENIX S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KARL-DEFLUX - Primary ID 08052747955329
Device Regulatory Overview
The KARL-DEFLUX (Model/Catalog Number: DE20301059) is a medical device manufactured by PHOENIX S.R.L.. This product is indexed under FDA Product Code / Category Classification A03010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DE20301059
- Product Code / EMDN
- A03010199
- Device Name
- Dispositivi per Infusione ed Aspirazione
- Database Sync Date
- 2026-08-09 16:46:06
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 KARL-DEFLUX?
The registered manufacturer of record for KARL-DEFLUX is PHOENIX S.R.L..
What is the Primary UDI-DI identifier for KARL-DEFLUX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052747955329.
What classification code is assigned to this device?
This device is registered under product classification code A03010199.
Similar Classification Devices (A03010199)
Other Devices by PHOENIX S.R.L.
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