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Liko Amputee HighBack Sling

by Liko Aktiebolag 5 variants

Ref 3575115

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 Number0887761GMN000038UD Basic UDI-DI 00887761983861UDI-DIDate17 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00887761983861 UDI-DI Date18 Jun 2020ListedStatusListed 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  • Withdrawn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
Liko Amputee HighBack Sling EUDAMED
Liko Amputee HighBack Sling™, Mod. 75 GUDID
Generic Name
Patient lifting system amputee sling
Device Name
Non-rigid body-support unit
Model / Reference
3575115
Primary DI / UDI-DI
00887761983861
Basic UDI-DI
0887761GMN000038UD
Direct Marketing DI
00887761983861
FDA Product Code
FSA
EMDN Code
V0805038002 Non-rigid supports for lifts (harnesses)
GMDN Term
Patient lifting system amputee sling
Device Class
Class I
Regulation Number
880.5510
EU market of registration
Sweden
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
SE-MF-000001404

Other devices from Liko Aktiebolag

See all devices from Liko Aktiebolag →

Properties

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