CONN, 3/16" X 3/16" W/O PART LINE 331011-000

GUDID B0663310110007

A sterile plastic device designed to join two or more tubes of a cardiopulmonary bypass system circuit, typically to create an extension or shunt; it

NOVOSCI CORP.

Cardiopulmonary bypass system tubing connector Cardiopulmonary bypass system tubing connector Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use Non-ISO80369-standardized small-bore multichannel connector, single-use
Primary Device IDB0663310110007
NIH Device Record Key8efb2ef1-bf31-47e1-b175-fee87632ec9d
Commercial Distribution StatusIn Commercial Distribution
Brand NameCONN, 3/16" X 3/16" W/O PART LINE
Version Model Number331011-000
Catalog Number331011-000
Company DUNS938289980
Company NameNOVOSCI CORP.
Device Count1
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latextrue
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB0663310110000 [Primary]
HIBCCB0663310110003 [Package]
Contains: B0663310110000
Package: INNER CARTON [25 Units]
In Commercial Distribution
HIBCCB0663310110005 [Package]
Contains: B0663310110000
Package: CASE [100 Units]
In Commercial Distribution
HIBCCB0663310110006 [Package]
Contains: B0663310110000
Package: PARTIAL CASE [50 Units]
In Commercial Distribution
HIBCCB0663310110007 [Package]
Contains: B0663310110000
Package: PARTIAL CASE [75 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KRIAccessory Equipment, Cardiopulmonary Bypass

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-10-12

On-Brand Devices [CONN, 3/16" X 3/16" W/O PART LINE]

B066331011NS5A sterile plastic device designed to join two or more tubes of a cardiopulmonary bypass system c
B0663310110007A sterile plastic device designed to join two or more tubes of a cardiopulmonary bypass system c
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.