CORFLO SAFETY PEG Kit 30-5320-S7

GUDID 20815149025388

PEG Safety Kit Pull Technique with snare

CORPAK MEDSYSTEMS, INC.

Gastrostomy tube
Primary Device ID20815149025388
NIH Device Record Keyee5683db-2d43-47aa-9e51-8a5a5be870c6
Commercial Distribution StatusIn Commercial Distribution
Brand NameCORFLO SAFETY PEG Kit
Version Model Number30-5320-S7
Catalog Number30-5320-S7
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

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110815149025381 [Primary]
GS120815149025388 [Package]
Contains: 10815149025381
Package: [2 Units]
In Commercial Distribution

FDA Product Code

KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20815149025388]

Ethylene Oxide


Device Entry Metadata

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

On-Brand Devices [CORFLO SAFETY PEG Kit]

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