eudamed_udi
Primary ID: 08049033190366
ONCOFUX (UDI 08049033190366)
Manufactured by Know Medical Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ONCOFUX - Primary ID 08049033190366
Device Regulatory Overview
The ONCOFUX (Model/Catalog Number: FL2 042 O) is a medical device manufactured by Know Medical Srl. This product is indexed under FDA Product Code / Category Classification A03010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FL2 042 O
- Product Code / EMDN
- A03010102
- Device Name
- ONCOFUX - Deflussore PUR per chemioterapia con 4 valvole needle-less
- Database Sync Date
- 2026-08-09 17:05:16
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 ONCOFUX?
The registered manufacturer of record for ONCOFUX is Know Medical Srl.
What is the Primary UDI-DI identifier for ONCOFUX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08049033190366.
What classification code is assigned to this device?
This device is registered under product classification code A03010102.
Similar Classification Devices (A03010102)
Other Devices by Know Medical Srl
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