AccessGUDID - DEVICE: Peritoneal Catheter (10381780037224)

GUDID

Device Identifier (DI) Information

Brand Name: Peritoneal Catheter
Version or Model: PC1
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: PC1
Company Name: INTEGRA NEUROSCIENCES IMPLANT (FRANCE)

Primary DI Number: 10381780037224
Issuing Agency: GS1
Commercial Distribution End Date: December 04, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 531408342 *Terms of Use

Device Description: The Integra NeuroSciences Peritoneal Catheter is a 91 cm silicone elastomer barium sulfate striped tubing. Numbered length markers are located 5, 10, 15, 20, 25 and 30 cm from the distal end to assist catheter placement. The distal end of the catheter has four staggered rows of 5.5-mm slits, which are not easily visible. If the distal outlet hole of the catheter becomes obstructed, the slits open for drainage.

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":	Yes
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 [?]
Premarket Submission Number Not Available/Not Released

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: ce5155f7-b5bd-4da3-b6a5-8a20e5f8711d
Public Version Date: March 18, 2024
Public Version Number: 4
DI Record Publish Date: October 01, 2015