AccessGUDID - DEVICE: CLOG Zapper Enteral Feeding tube Declogging System (10815149022069)

GUDID

Device Identifier (DI) Information

Brand Name: CLOG Zapper Enteral Feeding tube Declogging System
Version or Model: 20-0002
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 20-0002
Company Name: CORPAK MEDSYSTEMS, INC.

Primary DI Number: 10815149022069
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 147530323 *Terms of Use

Device Description: Declogging system for feeding tubes

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?
58939	Enteral feeding tube clearing kit	A collection of non-sterile compounds and devices intended to be used to prevent and/or remove, through biochemical action, an enteral formula clog in an in situ enteral feeding tube to maintain luminal patency. It typically includes a combination of enzymes, acids, and buffers (e.g., papain, cellulase, citric acid) and devices (e.g., syringe, tubing) to administer the cocktail into the enteral feeding tube. This is a single-patient device that may be reapplied to the patient for a limited number of times (single-use) before being discarded.	Active	false

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 00060443-88fb-4dae-8266-e21b86308382
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: August 04, 2016