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[ARVIS - Instruments] Instrument Tray

by Kico Knee Innovation Company Pty Ltd

Ref IN-19000

[ARVIS - Instruments] Instrument Tray (IN-19000) is a Class I device made by Kico Knee Innovation Company Pty Limited, registered in EUDAMED on 2 Sep 2025 (Basic UDI-DI 0888912000000S0104010A0RC), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0888912000000S0104010A0RC Basic UDI-DI 00810180351089UDI-DIDate2 Sep 2025RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 0888912000000S0104010A0RC — open Devices and search for it

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
[ARVIS - Instruments] Instrument Tray
Model / reference
IN-19000
Primary DI / UDI-DI
00810180351089
Basic UDI-DI
0888912000000S0104010A0RC
Direct marketing DI
00810180351089
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
AU-MF-000011477
Authorised representative
MedEnvoy Global BV NL-AR-000024028

Similar devices in this category

Other devices filed under TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.

Other devices from Kico Knee Innovation Company Pty Limited

  • Arvis ® In-21900 Open recall

    Class II

  • Arvis ® In-21904 Open recall

    Class II

  • Arvis ® In-21902 Open recall

    Class II

  • Arvis ® In-28000 Open recall

    Class II

See all devices from Kico Knee Innovation Company Pty Limited →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)