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Cranial Reference Frame A

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 950-NC-CRF-A

by ClaroNav Kolahi Inc

Identity

Trade Name
Cranial Reference Frame A EUDAMEDFDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
Navient Instruments EUDAMED
Cranial Reference Frame A for Navient FDA UDI
Model / Reference
950-NC-CRF-A EUDAMEDFDA UDI
Description
Cranial Reference Frame A for Navient FDA UDI

Identifiers

Primary DI / UDI-DI
07540209955327 EUDAMEDFDA UDI
Basic UDI-DI
7540209955-NC-REUSDA EUDAMED
Direct Marketing DI
07540209955327 EUDAMED
FDA Product Code
HAW FDA UDI
EMDN Code
Z12011480 SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES 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
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Neurological stereotactic surgery system

Cranial Reference Frame A by ClaroNav Kolahi Inc — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Neurological stereotactic surgery system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ClaroNav Kolahi Inc

Sources (2)

  • FDA UDI 76196836-61b0-434b-a4da-8915af328ef4 33 fields · synced Jul 17, 2026
  • EUDAMED 800820c1-361a-4e56-8d4b-015eb8fe3ef7 61 fields · synced Jul 17, 2026