eudamed_udi
Primary ID: 08033772321914
Smartflux LFP.180 PUREMA (UDI 08033772321914)
Manufactured by Medica S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Smartflux LFP.180 PUREMA - Primary ID 08033772321914
Device Regulatory Overview
The Smartflux LFP.180 PUREMA (Model/Catalog Number: M03535) is a medical device manufactured by Medica S.p.A.. This product is indexed under FDA Product Code / Category Classification F01060103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M03535
- Product Code / EMDN
- F01060103
- Device Name
- Dialyzers with KUF < 18 ml/h/mmHg
- Database Sync Date
- 2026-08-09 16:51:36
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 Smartflux LFP.180 PUREMA?
The registered manufacturer of record for Smartflux LFP.180 PUREMA is Medica S.p.A..
What is the Primary UDI-DI identifier for Smartflux LFP.180 PUREMA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033772321914.
What classification code is assigned to this device?
This device is registered under product classification code F01060103.
Similar Classification Devices (F01060103)
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