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Patient Loading Utility System (PLUS) P6601-01-076

by Lifeport, LLC.

Patient Loading Utility System (PLUS) P6601-01-076 is a Class I device made by Lifeport, LLC., listed in FDA GUDID since 14 Oct 2026 (UDI-DI 00810050863667), registry data as of 2 Nov 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810050863667 UDI-DI Date14 Oct 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Patient Loading Utility System (PLUS)
Generic name
Ambulance stretcher docking device
Model / reference
P6601-01-076
Primary DI / UDI-DI
00810050863667
FDA product code
FOX
GMDN term
Ambulance stretcher docking device
Device class
Class I
Regulation number
880.6990
GUDID distribution status
In Commercial Distribution

Other devices from Lifeport, LLC.

See all devices from Lifeport, LLC. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)