FDA UDI In Commercial Distribution 🇺🇸 United States

MoniTorrTM

DI: 10381780072003 · Model: SP0206 · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MoniTorrTM
Primary DI
10381780072003
Version / Model
SP0206
Catalog Number
SP0206
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-22
Public Version
5
Public Version Date
2020-09-22
Public Version Status
Update
Public Device Record Key
e0483c54-3a0c-46e6-a4b3-0eb9abd66786

Device Description

MONITORR ICP The MoniTorr ICP External CSF Drainage and Monitoring System provides a simple to use, closed system for the drainage of cerebrospinal fluid (CSF) from ventricles of the brain or the lumbar subarachnoid space to a drainage bag. The system may be used with a pole mounted assembly that allows for simple, quick, and accurate alignment with the patient and secure, positive or negative pressure level setting. The system has also been designed to provide for ease of patient transport through a compact design and an antimicrobial hydrophobic vent feature that resists occlusion. Common features include a calibrated graduated burette, a drainage bag, sampling/aspiration sites, and an increased green stripe pressure tubing.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JXG Shunt, central nervous system and components

GMDN Terms

Code Name
61798 Ventricular cerebrospinal fluid drainage catheterization kit
61797 Lumbar cerebrospinal fluid drainage catheterization kit

Identifiers

Type ID
Primary 10381780072003
Secondary M269SP02061

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K022554 000
K062599 000
K920156 000