CORFLO Safety PEG Kit 50-6312

GUDID 20815149021632

PEG Kit with ENFit Connectors Pull Technique

CORPAK MEDSYSTEMS, INC.

Gastrostomy tube
Primary Device ID20815149021632
NIH Device Record Key19dce27a-50f6-425d-8be8-beb253ff0840
Commercial Distribution StatusIn Commercial Distribution
Brand NameCORFLO Safety PEG Kit
Version Model Number50-6312
Catalog Number50-6312
Company DUNS147530323
Company NameCORPAK MEDSYSTEMS, INC.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(847)403-3400
Emailquestions@corpak.com

Device Dimensions

Catheter Gauge12 French

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *No

Device Identifiers

Device Issuing AgencyDevice ID
GS110815149021635 [Primary]
GS120815149021632 [Package]
Contains: 10815149021635
Package: [2 Units]
In Commercial Distribution

FDA Product Code

KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20815149021632]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-04-20
Device Publish Date2016-06-24

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