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Prism Air PAP100001

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00199874887180 UDI-DI Date10 Jul 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  • Withdrawn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 Air
Generic Name
Inflatable patient transfer sliding mattress, reprocessed
Model / Reference
PAP100001
Primary DI / UDI-DI
00199874887180
FDA Product Code
FRZ
GMDN Term
Inflatable patient transfer sliding mattress, reprocessed
Device Class
Class II
Regulation Number
880.6775
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Prism Pacific Industries LLC

See all devices from Prism Pacific Industries LLC →

Properties

  • Premarket Exempt
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • 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
  • Lot / Batch Number: No