GUDIDData
eudamed_udi Primary ID: D-868475920101NW

NephroFilter Low Uf (UDI D-868475920101NW)

Manufactured by NEPHROCAN MEDİKAL SANAYİ TİCARET ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NephroFilter Low Uf - Primary ID D-868475920101NW

Device Regulatory Overview

The NephroFilter Low Uf (Model/Catalog Number: NephroPS10R - 4210217) is a medical device manufactured by NEPHROCAN MEDİKAL SANAYİ TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification F01060103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NephroPS10R - 4210217
Product Code / EMDN
F01060103
Device Name
NephroFilter Low Uf
Database Sync Date
2026-08-09 16:50:45

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of NephroFilter Low Uf?

The registered manufacturer of record for NephroFilter Low Uf is NEPHROCAN MEDİKAL SANAYİ TİCARET ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for NephroFilter Low Uf?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-868475920101NW.

What classification code is assigned to this device?

This device is registered under product classification code F01060103.

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