Identity
- Trade Name
- LifePort® Kidney Transporter FDA UDI
- Generic Name
- Kidney donor-organ preservation/transport perfusion set FDA UDI
- Device Name
- LifePort® Kidney Transporter Sterile Drape - Perfusion Pack (Kit) FDA UDI
- Model / Reference
- LKT300 FDA UDI
- Description
- LifePort® Kidney Transporter Sterile Drape - Perfusion Pack (Kit) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815045020063 FDA UDI
- FDA Product Code
- KDL FDA UDI
- GMDN Term
- Kidney donor-organ preservation/transport perfusion set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5880 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
LifePort® Kidney Transporter by Organ Recovery Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Organ Recovery Systems, Inc.
Sources (1)
- FDA UDI 8e042445-6754-4b0b-99b5-e7fef0c72dcd 35 fields · synced Jun 9, 2026