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SlingOn

by Etac Immedia A/S 2 variants

Ref IM437/SModel Special Solutions

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number57080126001MM Basic UDI-DI 05708012481132UDI-DIDate9 May 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number05708012481132 UDI-DI Date31 Oct 2022ListedStatusListed 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  • Withdrawn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
SlingOn EUDAMED
Immedia GUDID
Generic Name
Patient transfer sliding mat
Model / Ref / Catalog
Special Solutions, IM437/S, SlingOn S
Primary DI / UDI-DI
05708012481132
Basic UDI-DI
57080126001MM
FDA Product Code
IKX
EMDN Code
Y122799 Non-motorized vehicles and means of transport - other
GMDN Term
Patient transfer sliding mat
Device Class
Class I
Regulation Number
890.5050
EU market of registration
Denmark
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Special Solutions
IM437/S
GUDID
SlingOn S

Manufacturer details

EUDAMED SRN
DK-MF-000019241

Other devices from Etac Immedia A/S

See all devices from Etac Immedia A/S →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (21)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No