Integra™ External Drainage System - The External CSF Drainage Systems provide a - Integra Lifesciences Corporation

Duns Number:083171244

Device Description: The External CSF Drainage Systems provide a sterile fluid path resistant to microbial part The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. The systems are used to drain CSF from ventricles of the brain or the lumbar subarachnoid space to a drainage bag. System components facilitate CSF drainage, fluid injection, CSF sampling and intracranial pressure monitoring.

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More Product Details

Catalog Number

NL8508601

Brand Name

Integra™ External Drainage System

Version/Model Number

NL8508601

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K972994

Product Code Details

Product Code

JXG

Product Code Name

Shunt, central nervous system and components

Device Record Status

Public Device Record Key

8ff00378-d0e8-4de3-a9a9-9ed3e3008ab8

Public Version Date

December 15, 2020

Public Version Number

5

DI Record Publish Date

September 22, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INTEGRA LIFESCIENCES CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 14
2 A medical device with a moderate to high risk that requires special controls. 75
3 A medical device with high risk that requires premarket approval 17
U Unclassified 32