CORFLO PEG Kit 30-6020

GUDID 20815149024138

PEG Kit Pull Technique

CORPAK MEDSYSTEMS, INC.

Gastrostomy tube
Primary Device ID20815149024138
NIH Device Record Keyea45335c-738d-42b2-a624-eb4de4e65a7e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCORFLO PEG Kit
Version Model Number30-6020
Catalog Number30-6020
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 Gauge20 French

Device Identifiers

Device Issuing AgencyDevice ID
GS110815149024131 [Primary]
GS120815149024138 [Package]
Contains: 10815149024131
Package: [2 Units]
In Commercial Distribution

FDA Product Code

KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20815149024138]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-04-20
Device Publish Date2016-08-04

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