eudamed_udi
Primary ID: 05420040801736
SUREFLUX (UDI 05420040801736)
Manufactured by NIPRO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SUREFLUX - Primary ID 05420040801736
Device Regulatory Overview
The SUREFLUX (Model/Catalog Number: SF-17E-GJ) is a medical device manufactured by NIPRO CORPORATION. This product is indexed under FDA Product Code / Category Classification F01060202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SF-17E-GJ
- Product Code / EMDN
- F01060202
- Device Name
- HEMODIALYZER
- Database Sync Date
- 2026-08-09 16:51:26
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 SUREFLUX?
The registered manufacturer of record for SUREFLUX is NIPRO CORPORATION.
What is the Primary UDI-DI identifier for SUREFLUX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05420040801736.
What classification code is assigned to this device?
This device is registered under product classification code F01060202.
Similar Classification Devices (F01060202)
Other Devices by NIPRO CORPORATION
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