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Prism Glide Half Mat PGH101035

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 Number00860016216020 UDI-DI Date12 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  • Withdrawn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 Glide Half Mat
Generic Name
Inflatable patient transfer sliding mattress, single-use
Model / Reference
PGH101035
Primary DI / UDI-DI
00860016216020
FDA Product Code
FRZ
GMDN Term
Inflatable patient transfer sliding mattress, single-use
Device Class
Class II
Regulation Number
880.6775
GUDID distribution status
In Commercial Distribution

Other devices from Prism Pacific Industries LLC

See all devices from Prism Pacific Industries LLC →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: 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