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Keypoint

FDA UDI

Class II (US FDA UDI)

by Natus Manufacturing Limited

Identity

Trade Name
Keypoint FDA UDI
Generic Name
Neurophysiologic monitoring system FDA UDI
Device Name
Focus Main Unit FDA UDI
Model / Reference
9033G0703 FDA UDI
Description
Focus Main Unit FDA UDI

Identifiers

Catalog Number
9033G0703 FDA UDI
Primary DI / UDI-DI
00382830050296 FDA UDI
510(k) Number
K140680 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neurophysiologic monitoring system

Keypoint by Natus Manufacturing Limited — 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

K140680 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Natus Manufacturing Limited

Sources (1)

  • FDA UDI 24f2cb9a-a035-43d2-9eb1-611c9d11f6ca 35 fields · synced May 30, 2026