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[ARVIS - Instruments] Tracker A, B, C

EUDAMEDFDA UDI

Class I (EU MDR)

Ref IN-10600

by Kico Knee Innovation Company Pty Ltd

Identity

Trade Name
ARVIS ® FDA UDI
Generic Name
Surgical optical-tracking spatial marker, reusable FDA UDI
Device Name
[ARVIS - Instruments] Tracker A, B, C EUDAMED
Tracker B FDA UDI
Model / Reference
IN-10600 EUDAMEDFDA UDI
Description
Tracker B FDA UDI

Identifiers

Primary DI / UDI-DI
00810180350693 EUDAMEDFDA UDI
Basic UDI-DI
08889120000Z120114800A4G5 EUDAMED
Direct Marketing DI
00810180350693 EUDAMED
FDA Product Code
OLO FDA UDI
EMDN Code
Z12011480 SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Surgical optical-tracking spatial marker, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Neurological stereotactic surgery system

[ARVIS - Instruments] Tracker A, B, C by Kico Knee Innovation Company Pty Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Neurological stereotactic surgery system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 9cf196a4-ba0e-4692-bb45-0e9b69e8a523 61 fields · synced Jul 29, 2026
  • FDA UDI be02a1e0-f846-45fa-8975-d34a981ae570 33 fields · synced May 30, 2026