eudamed_udi
Primary ID: 05420040810622
Diacap (UDI 05420040810622)
Manufactured by NIPRO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Diacap - Primary ID 05420040810622
Device Regulatory Overview
The Diacap (Model/Catalog Number: 7202217) is a medical device manufactured by NIPRO CORPORATION. This product is indexed under FDA Product Code / Category Classification F01060303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7202217
- Product Code / EMDN
- F01060303
- Device Name
- SYNTHETIC HEMODIALYZER
- Database Sync Date
- 2026-08-09 17:10:49
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 Diacap?
The registered manufacturer of record for Diacap is NIPRO CORPORATION.
What is the Primary UDI-DI identifier for Diacap?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05420040810622.
What classification code is assigned to this device?
This device is registered under product classification code F01060303.
Similar Classification Devices (F01060303)
Other Devices by NIPRO CORPORATION
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