eudamed_udi
Primary ID: 08033772327688
SPINFLUXTM 11 PUR LF (UDI 08033772327688)
Manufactured by Medica S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPINFLUXTM 11 PUR LF - Primary ID 08033772327688
Device Regulatory Overview
The SPINFLUXTM 11 PUR LF (Model/Catalog Number: SPINFLUXTM 11 PUR LF) 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
- SPINFLUXTM 11 PUR LF
- Product Code / EMDN
- F01060103
- Device Name
- Dialyzers with KUF < 18 ml/h/mmHg
- Database Sync Date
- 2026-08-09 16:59:20
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 SPINFLUXTM 11 PUR LF?
The registered manufacturer of record for SPINFLUXTM 11 PUR LF is Medica S.p.A..
What is the Primary UDI-DI identifier for SPINFLUXTM 11 PUR LF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033772327688.
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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