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microTargeting™ Electrode Sterilization Tray

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
microTargeting™ Electrode Sterilization Tray FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
microTargeting Electrode Sterilization Tray FDA UDI
Model / Reference
67-00-1-00261 FDA UDI
Description
microTargeting Electrode Sterilization Tray FDA UDI

Identifiers

Catalog Number
67-00-1 FDA UDI
Primary DI / UDI-DI
00873263002612 FDA UDI
510(k) Number
K033173 FDA UDI
FDA Product Code
GZL FDA UDI
GMDN Term
Surgical instrument/implant rack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1330 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

microTargeting™ Electrode Sterilization Tray by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 679dd7b6-136e-4c3f-900d-42104741f9b7 37 fields · synced May 30, 2026