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LifePort® Kidney Transporter

FDA UDI

Class II (US FDA UDI)

by Organ Recovery Systems, Inc.

Identity

Trade Name
LifePort® Kidney Transporter FDA UDI
Generic Name
General-purpose donor-organ preservation/transport system FDA UDI
Device Name
LifePort® Kidney Transporter 1.1 FDA UDI
Model / Reference
LKT101P FDA UDI
Description
LifePort® Kidney Transporter 1.1 FDA UDI

Identifiers

Primary DI / UDI-DI
00815045020018 FDA UDI
510(k) Number
K021362 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

LifePort® Kidney Transporter by Organ Recovery Systems, 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9b3ca745-f215-42e0-a67f-f270c6d7cb15 34 fields · synced Jun 9, 2026