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microTargeting™ STar™ Array Insertion Tube Extractor

FDA UDI

Class I (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
microTargeting™ STar™ Array Insertion Tube Extractor FDA UDI
Generic Name
Intracerebral cannula, implantable FDA UDI
Device Name
microTargeting STar Array Insertion Tube Extractor, 5x, Sterile, for use the STar Array Insertion Tubes FDA UDI
Model / Reference
70-CN-ET-00236 FDA UDI
Description
microTargeting STar Array Insertion Tube Extractor, 5x, Sterile, for use the STar Array Insertion Tubes FDA UDI

Identifiers

Catalog Number
70-CN-ET FDA UDI
Primary DI / UDI-DI
00873263002360 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Intracerebral cannula, implantable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Intracerebral cannula, implantable

microTargeting™ STar™ Array Insertion Tube Extractor by Fhc, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intracerebral cannula, implantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI 292bd06e-d159-4249-972b-9b94849f3ce4 36 fields · synced Jun 1, 2026