DEVICE: CODMAN® BACTISEAL® (10381780537069)
Device Identifier (DI) Information
CODMAN® BACTISEAL®
NS0339
In Commercial Distribution
NS0339
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
NS0339
In Commercial Distribution
NS0339
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
CODMAN® BACTISEAL® Clear with Barium Stripe Distal Catheter 120cm
MR Conditional Contents: Distal Catheter 120cm (1)
Device Characteristics
| MR Conditional | |
| No | |
| No | |
| Yes | |
| Yes | |
| No | |
| No | |
| Yes | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 61159 | Peritoneal/atrial cerebrospinal fluid catheter |
A flexible tube intended to be implanted as the distal component of a ventriculo-peritoneal/atrial shunt, to channel cerebrospinal fluid (CSF) to either the peritoneal cavity or the right atrium (i.e., dual-capability) where it can be absorbed into the body. It is intended to be part of a therapeutic measure for situations where excess CSF causes elevated intracranial pressure (hydrocephalus). Disposable devices associated with implantation may be included.
|
Active | true |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| HCA | CATHETER, VENTRICULAR |
| JXG | Shunt, central nervous system and components |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| Premarket Submission Number Not Available/Not Released | |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Storage Environment Temperature: between 2 and 27 Degrees Celsius |
| Handling Environment Temperature: between 2 and 27 Degrees Celsius |
| Handling Environment Temperature: between 36 and 81 Degrees Fahrenheit |
| Storage Environment Temperature: between 36 and 81 Degrees Fahrenheit |
| Special Storage Condition, Specify: Do not use if package is damaged, Keep away from sunlight |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Catheter Length: 120 Centimeter |
Device Record Status
dad41968-cf9d-4ba7-a7f6-2c4691d3e62b
March 24, 2025
2
November 20, 2024
March 24, 2025
2
November 20, 2024
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)654-2873
custsvcnj@integralife.com
custsvcnj@integralife.com