← Back to catalogue

Patient Loading Utility System (PLUS)

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name
Patient Loading Utility System (PLUS) FDA UDI
Generic Name
Ambulance stretcher docking device FDA UDI
Device Name
ASSEMBLY - PLUS – MAJOR * PATIENT LOADING UTILITY SYSTEM FDA UDI
Model / Reference
0403-0111-04-01-16 FDA UDI
Description
ASSEMBLY - PLUS – MAJOR * PATIENT LOADING UTILITY SYSTEM FDA UDI

Identifiers

Primary DI / UDI-DI
00810050861533 FDA UDI
FDA Product Code
FOX FDA UDI
BTI FDA UDI
CAN FDA UDI
BXO FDA UDI
GMDN Term
Ambulance stretcher docking device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 FDA UDI
868.6250 FDA UDI
868.2700 FDA UDI
868.2900 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

Yes

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: Non-fixed medical gas cylinder regulatorAmbulance stretcher docking deviceAir/gas pressure transducerLaboratory pump, vacuum

Patient Loading Utility System (PLUS) by Lifeport, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory pump, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Lifeport, Llc.

Sources (1)

  • FDA UDI 317f0b08-e795-47c3-80a6-fbaa16e3747c 34 fields · synced Jun 8, 2026