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Universal Tracker for Stimulation Probe

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 950-NC-UTSP

by Claronav Kolahi

Identity

Trade Name
Universal Tracker for Stimulation Probe EUDAMED
Universal Tracker Stimulation probe FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
Disposable Instruments EUDAMED
Universal Tracker Stimulation probe for use with Navient system, cranial FDA UDI
Model / Reference
950-NC-UTSP EUDAMEDFDA UDI
Description
Universal Tracker Stimulation probe for use with Navient system, cranial FDA UDI

Identifiers

Primary DI / UDI-DI
07540209955747 EUDAMEDFDA UDI
Basic UDI-DI
7540209955-NC-DINSTQM EUDAMED
510(k) Number
K241327 FDA UDI
FDA Product Code
HAW FDA UDI
EMDN Code
Z12011485 SURGICAL NAVIGATION INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Neurological stereotactic surgery system FDA UDI

Classification

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

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Universal Tracker for Stimulation Probe by Claronav Kolahi — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Claronav Kolahi
EUDAMED SRN
CA-MF-000037841
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 3472a4fd-9f9b-4c50-812c-60c709789d84 61 fields · synced Jul 17, 2026
  • FDA UDI 4e0180df-e6b2-437a-a522-126e2c0a74c4 34 fields · synced May 30, 2026