AccessGUDID - DEVICE: CORFLO Jejunal Feeding Tube (10815149020775)

GUDID

Device Identifier (DI) Information

Brand Name: CORFLO Jejunal Feeding Tube
Version or Model: 50-7368
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 50-7368
Company Name: CORPAK MEDSYSTEMS, INC.

Primary DI Number: 10815149020775
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 147530323 *Terms of Use

Device Description: Jejunal Tube with ENFit Connectors 3 g weighted with stylet for use with CORFLO PEG

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
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?
38564	Jejunostomy tube	A sterile, thin, flexible, hollow tube percutaneously inserted into the jejunum, typically through puncture of the abdominal wall and stomach after distention of the gut by endoscopic methods. It is used to feed a patient who has a physical disability that prevents oral feeding (e.g., a birth defect of the mouth, oesophagus, or stomach, or a neuromuscular condition that affects chewing and swallowing), and/or to provide drainage/decompression for the stomach when it is necessary to bypass a longstanding obstruction of the stomach outlet into the small intestine. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
KNT	TUBES, GASTROINTESTINAL (AND ACCESSORIES)

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: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: No

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 8 FR (2.7mm) X 36" (91cm)
Length: 36 Inch
Catheter Gauge: 8 French

Device Record Status

Public Device Record Key: acf7f265-3423-42c5-b448-e6b82ec038ed
Public Version Date: October 07, 2019
Public Version Number: 3
DI Record Publish Date: June 24, 2016