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Plus

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name
PLUS FDA UDI
Generic Name
Ambulance stretcher docking device FDA UDI
Device Name
ASSEMBLY, PLUS, PC-24 FDA UDI
Model / Reference
P7210-01-001 FDA UDI
Description
ASSEMBLY, PLUS, PC-24 FDA UDI

Identifiers

Primary DI / UDI-DI
00810050861083 FDA UDI
FDA Product Code
FOX FDA UDI
BTI FDA UDI
CAN FDA UDI
GCX 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
880.6740 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: Non-fixed medical gas cylinder regulatorMedical device air compressorAmbulance stretcher docking deviceLaboratory pump, vacuum

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

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Manufacturer

Manufacturer
Lifeport, Llc.

Sources (1)

  • FDA UDI bed3e8c8-3a06-44ca-9f61-f17a0168eea4 34 fields · synced May 31, 2026