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Prism Lift Seated Sling PLS1000EX

by Prism Pacific Industries LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860012736089 UDI-DI Date27 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Prism Lift Seated Sling
Generic Name
General-purpose patient lifting system sling/harness
Model / Reference
PLS1000EX
Primary DI / UDI-DI
00860012736089
FDA Product Code
FMR
GMDN Term
General-purpose patient lifting system sling/harness
Device Class
Class I
Regulation Number
880.6785
GUDID distribution status
In Commercial Distribution

Other devices from Prism Pacific Industries LLC

See all devices from Prism Pacific Industries LLC →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No