ADULT TIP SUCKER HEX HANDLE WITH VENT 201280NS

GUDID B066201280NS1

An assembly of devices designed to evacuate fluid, tissue, gas, or other foreign materials from a body cavity or lumen by means of suction. It general

NOVOSCI CORP.

General-purpose suction system, pneumatic
Primary Device IDB066201280NS1
NIH Device Record Keyd1765c35-6b08-4d24-8c9c-584e3493633a
Commercial Distribution StatusIn Commercial Distribution
Brand NameADULT TIP SUCKER HEX HANDLE WITH VENT
Version Model Number201280NS
Catalog Number201280NS
Company DUNS938289980
Company NameNOVOSCI CORP.
Device Count100
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com
Phone800-854-0567
Emailinfo@novosci.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB066201280NS0 [Unit of Use]
HIBCCB066201280NS1 [Primary]
HIBCCB066201280NS3 [Package]
Package: INNER BAG [50 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DTSSucker, Cardiotomy Return, Cardiopulmonary Bypass

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


[B066201280NS1]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-10-06

Devices Manufactured by NOVOSCI CORP.

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B066341222NS1 - CONNECTOR, Y 1/4" X 1/4" X 1/4"2022-03-10 A plastic device designed to join two or more tubes of a cardiopulmonary bypass system circuit, typically to create an extension
B066341344NS5 - CONNECTOR, Y 3/8" x 1/2" x 1/2" W/O LUER2022-03-10 A plastic device designed to join two or more tubes of a cardiopulmonary bypass system circuit, typically to create an extension
B066H11360 - STANDARD VAVD KIT2022-03-10 A collection of sterile devices intended to be used to inject cardioplegia solution into the heart to interrupt its contractions
B0663011240000 - QUICKIE PRIME - 24" W/CLAMP2022-03-09 A sterile, semi-rigid tube used in open heart surgery to facilitate the transfer of priming fluids during the priming of the ext

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