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Sling - Loop Ambulation

by ArjoHuntleigh AB

Ref MLA5100-MModel NPA0500, KKX522900L

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number5060693520204VR Basic UDI-DI 05059441380467UDI-DIDate8 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05059441380467 UDI-DI Date9 Mar 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Sling - Loop Ambulation EUDAMED
Arjo Loop Ambulation Sling GUDID
Generic Name
General-purpose patient lifting system sling/harness
Device Name
Disposable Slide Sheet
Sling - Standing
Model / Ref / Catalog
NPA0500, MLA5100-M, KKX522900L
Primary DI / UDI-DI
05059441380467
Basic UDI-DI
5060693520204VR, 5060693520150VT
FDA Product Code
FSA
EMDN Code
V0805038002 Non-rigid supports for lifts (harnesses)
GMDN Term
General-purpose patient lifting system sling/harness
Device Class
Class I
Regulation Number
880.5510
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
SE-MF-000000696

Other devices from Arjohuntleigh AB

See all devices from Arjohuntleigh AB →

Properties

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

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No