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KidneyVault

FDA UDI

Class II (US FDA UDI)

by Paragonix Technologies, Inc.

Identity

Trade Name
KidneyVault FDA UDI
Generic Name
General-purpose donor-organ preservation/transport system FDA UDI
Device Name
KidneyVault Cannula Multi-Pack (3, 5, 7, 9, 7x20, 10x35) FDA UDI
Model / Reference
PRGNX-8008-010 FDA UDI
Description
KidneyVault Cannula Multi-Pack (3, 5, 7, 9, 7x20, 10x35) FDA UDI

Identifiers

Primary DI / UDI-DI
00850005470625 FDA UDI
FDA Product Code
KDN FDA UDI
GMDN Term
General-purpose donor-organ preservation/transport system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose donor-organ preservation/transport system

KidneyVault by Paragonix Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose donor-organ preservation/transport system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 30e930c3-4167-4165-9f95-03535ac87bd7 33 fields · synced Jun 9, 2026