gudid
Primary ID: RFP-220-A
NxStage PureFlow Solution (UDI RFP-220-A)
Manufactured by NXSTAGE MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NxStage PureFlow Solution - Primary ID RFP-220-A
Device Regulatory Overview
The NxStage PureFlow Solution (Model/Catalog Number: RFP-220-A) is a medical device manufactured by NXSTAGE MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification KPO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RFP-220-A
- Product Code / EMDN
- KPO
- Device Name
- Database Sync Date
- 2026-08-09 09:20:32
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 NxStage PureFlow Solution?
The registered manufacturer of record for NxStage PureFlow Solution is NXSTAGE MEDICAL, INC..
What is the Primary UDI-DI identifier for NxStage PureFlow Solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RFP-220-A.
What classification code is assigned to this device?
This device is registered under product classification code KPO.
Similar Classification Devices (KPO)
Other Devices by NXSTAGE MEDICAL, INC.
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