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Tracer Pointer

FDA UDI

Class II (US FDA UDI)

by Medtronic Navigation, Inc.

Identity

Trade Name
Tracer Pointer FDA UDI
Generic Name
Stereotactic surgery system probe, single-use FDA UDI
Device Name
POINTER 9735317 TRACER AXIEM PACKAGED FDA UDI
Model / Reference
9735317 FDA UDI
Description
POINTER 9735317 TRACER AXIEM PACKAGED FDA UDI

Identifiers

Primary DI / UDI-DI
00643169490024 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Stereotactic surgery system probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Stereotactic surgery system probe, single-use

Tracer Pointer by Medtronic Navigation, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stereotactic surgery system probe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bed47550-0710-4898-bc6f-224e7e4e6909 35 fields · synced May 30, 2026