Identity
- Trade Name
- Patient Loading Utility System (PLUS) FDA UDI
- Generic Name
- Ambulance stretcher docking device FDA UDI
- Device Name
- PLUS, 48 IN BAY WITH 6 IN CANTILEVER STRUCTURE FDA UDI
- Model / Reference
- P5401-01-003 FDA UDI
- Description
- PLUS, 48 IN BAY WITH 6 IN CANTILEVER STRUCTURE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810050862189 FDA UDI
- FDA Product Code
- FOX FDA UDIBTI FDA UDIGCX FDA UDI
- GMDN Term
- Ambulance stretcher docking device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6990 FDA UDI868.6250 FDA UDI880.6740 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
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Medical device air compressorAmbulance stretcher docking deviceLaboratory pump, vacuum
Patient Loading Utility System (PLUS) by Lifeport, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Laboratory pump, vacuum.
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- Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
- Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Lifeport, Llc.
Sources (1)
- FDA UDI 066ee587-a601-48fd-8f81-1ecd98ff1e18 34 fields · synced May 31, 2026