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Mölnlycke®Z-Flo™ Fluidized Positioner 1400522

by Mölnlycke Health Care AB

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 Number07333350455873 UDI-DI Date22 Sep 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  • Withdrawn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
Mölnlycke®Z-Flo™ Fluidized Positioner
Generic Name
Freestanding patient positioner, single-use
Model / Reference
1400522
Primary DI / UDI-DI
07333350455873
FDA Product Code
FMP
GMDN Term
Freestanding patient positioner, single-use
Device Class
Class I
Regulation Number
880.6450
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Other devices from Mölnlycke Health Care AB

See all devices from Mölnlycke Health Care AB →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Expiration 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
  • Manufacturing Date: No