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Arjo Loop Ambulation Sling MFA5200

by Arjohuntleigh, 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 Number05059441456322 UDI-DI Date23 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  • Withdrawn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
Arjo Loop Ambulation Sling
Generic Name
General-purpose patient lifting system sling/harness
Model / Ref / Catalog
MFA5200
Primary DI / UDI-DI
05059441456322
FDA Product Code
FSA
GMDN Term
General-purpose patient lifting system sling/harness
Device Class
Class I
Regulation Number
880.5510
GUDID distribution status
In Commercial Distribution

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Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (9)

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