eudamed_udi
Primary ID: 04260748180181
florio NEPHREE (UDI 04260748180181)
Manufactured by Florio GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for florio NEPHREE - Primary ID 04260748180181
Device Regulatory Overview
The florio NEPHREE (Model/Catalog Number: not applicable) is a medical device manufactured by Florio GmbH. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- not applicable
- Product Code / EMDN
- V92
- Device Name
- florio NEPHREE
- Database Sync Date
- 2026-08-09 16:29:57
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 florio NEPHREE?
The registered manufacturer of record for florio NEPHREE is Florio GmbH.
What is the Primary UDI-DI identifier for florio NEPHREE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260748180181.
What classification code is assigned to this device?
This device is registered under product classification code V92.
Similar Classification Devices (V92)
Other Devices by Florio GmbH
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