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Natus®

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name
Natus® FDA UDI
Generic Name
Ventriculo-peritoneal/atrial shunt FDA UDI
Device Name
Gravity Compensating Accessory, Low Pressure Range (White) FDA UDI
Model / Reference
NT903430 FDA UDI
Description
Gravity Compensating Accessory, Low Pressure Range (White) FDA UDI

Identifiers

Catalog Number
NT903430 FDA UDI
Primary DI / UDI-DI
00382830056076 FDA UDI
510(k) Number
K152897 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Ventriculo-peritoneal/atrial shunt FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5550 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Ventriculo-peritoneal/atrial shunt

Natus® by Natus Medical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventriculo-peritoneal/atrial shunt.

Cleared under the same submission

K152897 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Natus Medical Incorporated

Sources (1)

  • FDA UDI 44905eab-967c-4f8d-b506-99d7e07c0722 37 fields · synced May 31, 2026