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Natus®

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name
Natus® FDA UDI
Generic Name
Cerebrospinal fluid shunt connector FDA UDI
Device Name
Lumbar-Peritoneal Shunt Stainless Steel Connector FDA UDI
Model / Reference
NT75121S06 FDA UDI
Description
Lumbar-Peritoneal Shunt Stainless Steel Connector FDA UDI

Identifiers

Catalog Number
NT75121S06 FDA UDI
Primary DI / UDI-DI
00382830057103 FDA UDI
510(k) Number
K811288 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Cerebrospinal fluid shunt connector 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

Category: Cerebrospinal fluid shunt connector

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

Similar devices

Also classified as Cerebrospinal fluid shunt connector.

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 524ff1b0-391c-4581-baa2-2f175ef8abc7 37 fields · synced May 29, 2026