eudamed_udi
Primary ID: 04968420722734
ELISIO (UDI 04968420722734)
Manufactured by NIPRO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELISIO - Primary ID 04968420722734
Device Regulatory Overview
The ELISIO (Model/Catalog Number: ELI-21M-GC) is a medical device manufactured by NIPRO CORPORATION. This product is indexed under FDA Product Code / Category Classification F01060203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ELI-21M-GC
- Product Code / EMDN
- F01060203
- Device Name
- SYNTHETIC HEMODIALYZER
- Database Sync Date
- 2026-08-09 16:51:18
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 ELISIO?
The registered manufacturer of record for ELISIO is NIPRO CORPORATION.
What is the Primary UDI-DI identifier for ELISIO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04968420722734.
What classification code is assigned to this device?
This device is registered under product classification code F01060203.
Similar Classification Devices (F01060203)
Other Devices by NIPRO CORPORATION
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