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Natus®

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name
Natus® FDA UDI
Generic Name
Ventriculoperitoneal shunt FDA UDI
Device Name
Novus™ Valve Shunt Kit, Standard, Low Pressure FDA UDI
Model / Reference
NT8509610 FDA UDI
Description
Novus™ Valve Shunt Kit, Standard, Low Pressure FDA UDI

Identifiers

Catalog Number
NT8509610 FDA UDI
Primary DI / UDI-DI
00382830056496 FDA UDI
510(k) Number
K153041 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Ventriculoperitoneal 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: Ventriculoperitoneal shunt

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

Similar devices

Also classified as Ventriculoperitoneal shunt.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9faeb3ab-77b7-449f-8951-60e9bbafe0b4 36 fields · synced Jun 8, 2026