NS0339
Integra Codman Bactiseal Peritoneal Catheter 120cm, Clear w/Barium Stripe
$29.00
box of 1
In Stock: 1 Each
Expiration:
Expired
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The item listed above is expired and may be used for educational, training, and non-clinical research purposes only. Any product information appearing below, including the product indication statement, pertains to an in-date item only.
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Description
Integra Codman Bactiseal Shunt Catheter System
For use in the treatment of hydrocephalus as a component of a shunt system when draining or shunting of cerebrospinal fluid (CSF) is indicated.
Product Code: NS0339
- Distal Catheter: 120cm
- Clear
- Barium
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
- Single-Use
- Disposable
Additional Details
- Company Name: Integra Lifesciences Production Corporation
- FDA Product Code: HCA
- FDA Product Code Name: Catheter, Ventricular
- FDA Product Code: JXG
- FDA Product Code Name: Shunt, central nervous system and components
- GMDN Term Code: 61159
- GMDN Term Name: Peritoneal/atrial cerebrospinal fluid catheter
- GMDN Term Definition: 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.
Additional information
| Size | 1 |
|---|---|
| Arms | N/A |
| Manufacturer | |
| Unit | box of 1 |
- FDA Product Code: HCA JXG
- FDA Product Code Name: Catheter, Ventricular / Shunt, Central Nervous System And Components
- GMDN Term Code: 61159
- GMDN Term Name: Peritoneal/atrial cerebrospinal fluid catheter
- GMDN Term Description: 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.
