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Natus®

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name
Natus® FDA UDI
Generic Name
Intracerebral infusion/drainage catheter, long-term FDA UDI
Device Name
Straight Ventricular Catheter F8, 15 cm, With Radiopaque Length Dots FDA UDI
Model / Reference
NT9MD102A FDA UDI
Description
Straight Ventricular Catheter F8, 15 cm, With Radiopaque Length Dots FDA UDI

Identifiers

Catalog Number
NT9MD102A FDA UDI
Primary DI / UDI-DI
00382830055604 FDA UDI
510(k) Number
K960159 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Intracerebral infusion/drainage catheter, long-term 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: Intracerebral infusion/drainage catheter, long-term

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

Similar devices

Also classified as Intracerebral infusion/drainage catheter, long-term.

Cleared under the same submission

K960159 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 394f72a8-7fd5-465b-8c7d-92ee98e50a3e 37 fields · synced May 30, 2026