AccessGUDID - DEVICE: Peritoneal Catheter (10381780034308)

GUDID

Device Identifier (DI) Information

Brand Name: Peritoneal Catheter
Version or Model: 953101
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 953101
Company Name: INTEGRA NEUROSCIENCES IMPLANT (FRANCE)

Primary DI Number: 10381780034308
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 531408342 *Terms of Use

Device Description: The peritoneal catheter is used to drain cerebrospinal fluid from the outlet of the valve unit into the peritoneum. The distal end of the catheter has four staggered rows of 6-mm slits, which are not readily visible. If the distal outlet hole of the catheter becomes obstructed, the slits open for drainage. The slits perform optimally in a saline environment after soaking for 24 hours at 37 degrees Celsius.

Device Characteristics

What MRI safety information does the labeling contain?	MR Safe
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

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
JXG	Shunt, central nervous system and components

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K861377	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 91cm Length x 2.3mm O.D. x 1.1mm I.D. (F7)

Device Record Status

Public Device Record Key: 1757e91d-b2d9-4407-8e4b-728ae1aeee1b
Public Version Date: February 09, 2023
Public Version Number: 6
DI Record Publish Date: October 01, 2015