← Back to catalogue

Guideline 4000 5.0™ microTargeting™ Controller Card

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
Guideline 4000 5.0™ microTargeting™ Controller Card FDA UDI
Generic Name
Neurophysiologic monitoring system FDA UDI
Device Name
GL5 Integrated microTargeting Controller FDA UDI
Model / Reference
C0223-00683 FDA UDI
Description
GL5 Integrated microTargeting Controller FDA UDI

Identifiers

Catalog Number
C0223 FDA UDI
Primary DI / UDI-DI
00873263006832 FDA UDI
510(k) Number
K183123 FDA UDI
FDA Product Code
GZL FDA UDI
GMDN Term
Neurophysiologic monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1330 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Neurophysiologic monitoring system

Guideline 4000 5.0™ microTargeting™ Controller Card by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurophysiologic monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI 05f221e8-7019-4b9a-baf6-1f4508338102 37 fields · synced May 30, 2026