CORFLO PEG Kit 50-6512

GUDID 20815149021670

PEG Kit with ENFit connectors basic components Pull Technique

CORPAK MEDSYSTEMS, INC.

Gastrostomy tube
Primary Device ID20815149021670
NIH Device Record Key0b0c2774-6880-4246-8277-0fd7b262eb6e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCORFLO PEG Kit
Version Model Number50-6512
Catalog Number50-6512
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
GS110815149021673 [Primary]
GS120815149021670 [Package]
Contains: 10815149021673
Package: [2 Units]
In Commercial Distribution

FDA Product Code

KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20815149021670]

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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