CORFLO cuBBy Decompression Set 56-0112

GUDID 20815149022868

Decompression set for use with CORFLO cuBBy

CORPAK MEDSYSTEMS, INC.

Enteral tube extension
Primary Device ID20815149022868
NIH Device Record Keyf68bf237-8ed3-4194-90bc-af6d47311f33
Commercial Distribution Discontinuation2021-08-06
Commercial Distribution StatusNot in Commercial Distribution
Brand NameCORFLO cuBBy Decompression Set
Version Model Number56-0112
Catalog Number56-0112
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 Kitfalse
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
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No
Special Storage Condition, SpecifyBetween 0 and 0 *No

Device Identifiers

Device Issuing AgencyDevice ID
GS110815149022861 [Primary]
GS120815149022868 [Package]
Contains: 10815149022861
Package: [5 Units]
Discontinued: 2021-08-06
Not in Commercial Distribution

FDA Product Code

KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2023-07-31
Device Publish Date2016-06-24

Devices Manufactured by CORPAK MEDSYSTEMS, INC.

20815149021144 - CORGRIP Tube Retention System2023-07-31 retention system for NG feeding tubes
20815149021151 - CORGRIP Tube Retention System2023-07-31 retention system for NG feeding tubes
20815149021168 - CORGRIP Tube Retention System2023-07-31 retention system for NG feeding tubes
20815149021731 - CORFLO Y Extension Set2023-07-31 Enteral feeding extension set.
20815149022868 - CORFLO cuBBy Decompression Set2023-07-31Decompression set for use with CORFLO cuBBy
20815149022868 - CORFLO cuBBy Decompression Set2023-07-31 Decompression set for use with CORFLO cuBBy
20815149022875 - CORFLO cuBBy Right Angle Feeding Set2023-07-31 Feeding set for use with CORFLO cuBBy with ENFit connectors
20815149022882 - CORFLO cuBBy Right Angle Feeding Set2023-07-31 Feeding set for use with CORFLO cuBBy with ENFit connectors
20815149024442 - CORFLO cuBBy2023-07-31 Feeding set for use with CORFLO cuBBy

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