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STar™ Drive SteriSuite Case

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
STar™ Drive SteriSuite Case FDA UDI
Generic Name
Neurosurgical micro targeting drive FDA UDI
Device Name
Sterilzation Wire Basket for STar(TM) Drive System FDA UDI
Model / Reference
67-00-7-00299 FDA UDI
Description
Sterilzation Wire Basket for STar(TM) Drive System FDA UDI

Identifiers

Catalog Number
67-00-7 FDA UDI
Primary DI / UDI-DI
00873263002995 FDA UDI
510(k) Number
K092562 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Neurosurgical micro targeting drive 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

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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Neurosurgical micro targeting drive

STar™ Drive SteriSuite Case by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical micro targeting drive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI 53270da9-a799-4b56-8610-1025b2f73c4a 37 fields · synced May 31, 2026