← Back to catalogue

Utility Pedestal Assembly

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name
Utility Pedestal Assembly FDA UDI
Generic Name
Ambulance stretcher docking device FDA UDI
Device Name
16G UTILITY PEDESTAL FDA UDI
Model / Reference
ST2-271-01-004 FDA UDI
Description
16G UTILITY PEDESTAL FDA UDI

Identifiers

Primary DI / UDI-DI
00810050861809 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

Utility Pedestal Assembly 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 04ef3cb9-78b6-4fae-ba9b-8f81adab0bec 34 fields · synced May 30, 2026