Primary Device ID | 10381780071693 |
NIH Device Record Key | fe66ac03-6b49-475e-a62c-5d90b37d5554 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Integra™ External Drainage System |
Version Model Number | NL8508600 |
Catalog Number | NL8508600 |
Company DUNS | 083171244 |
Company Name | Integra Lifesciences Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 10381780071693 [Primary] |
HIBCC | M269NL85086001 [Secondary] |
JXG | Shunt, central nervous system and components |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-09-22 |
Device Publish Date | 2015-09-22 |
10381780071709 | The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. |
10381780071693 | The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. |