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omniTRAX Patient Tracker

FDA UDI

Class II (US FDA UDI)

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
omniTRAX Patient Tracker FDA UDI
Generic Name
Electromagnetic device tracking system spatial marker FDA UDI
Device Name
Reusable non-sterile multi-modality fiducial marker with CIVCO general purpose sensor connection FDA UDI
Model / Reference
610-1228 FDA UDI
Description
Reusable non-sterile multi-modality fiducial marker with CIVCO general purpose sensor connection FDA UDI

Identifiers

Catalog Number
610-1228 FDA UDI
Primary DI / UDI-DI
10841436102640 FDA UDI
510(k) Number
K092619 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Electromagnetic device tracking system spatial marker FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 2.8 Inch FDA UDI
Width — 2.8 Inch FDA UDI

Category: Electromagnetic device tracking system spatial marker

omniTRAX Patient Tracker by Civco Medical Instruments Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromagnetic device tracking system spatial marker.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d7290b6-2474-4ad1-ba53-258507b12c3e 38 fields · synced Jun 8, 2026