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Pro-Daptive SensorCell Flotation Surface PDA-9100-4280

by Levisense Medical, Inc.

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 NumberG771PDA91004280 UDI-DI Date15 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  • Withdrawn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
Pro-Daptive SensorCell Flotation Surface
Generic Name
Alternating-pressure bed mattress system
Model / Ref / Catalog
PDA-9100-4280, MA
Primary DI / UDI-DI
G771PDA91004280
FDA Product Code
FNM
GMDN Term
Alternating-pressure bed mattress system
Device Class
Class II
Regulation Number
880.5550
GUDID distribution status
In Commercial Distribution
Size
Length — 80 Inch
Width — 42 Inch

Other devices from Levisense Medical, Inc.

Properties

  • Contains Latex
  • Over-the-Counter
  • Premarket Exempt
  • Serial Number

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No