Blue Vessel Clamp 201003-000

GUDID B0662010030006

A sterile, hand-held manual surgical instrument designed to directly compress a blood vessel (vein or artery) to create a temporary haemostasis (arres

NOVOSCI CORP.

Vascular clamp, single-use Vascular clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use
Primary Device IDB0662010030006
NIH Device Record Key0f541c45-77ee-47cd-9aef-51e2369ee462
Commercial Distribution StatusIn Commercial Distribution
Brand NameBlue Vessel Clamp
Version Model Number201003-00
Catalog Number201003-000
Company DUNS938289980
Company NameNOVOSCI CORP.
Device Count1
DM Exemptfalse
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 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
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
HIBCCB0662010030000 [Primary]
HIBCCB0662010030003 [Package]
Contains: B2010030000
Package: Inner Carton [25 Units]
In Commercial Distribution
HIBCCB0662010030004 [Package]
Contains: B2010030000
Package: Partial Case [50 Units]
In Commercial Distribution
HIBCCB0662010030005 [Package]
Contains: B2010030000
Package: Partial Case [75 Units]
In Commercial Distribution
HIBCCB0662010030006 [Package]
Contains: B2010030000
Package: Case [100 Units]
In Commercial Distribution
HIBCCB2010030000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-26

On-Brand Devices [Blue Vessel Clamp]

B0662010030006A sterile, hand-held manual surgical instrument designed to directly compress a blood vessel (ve
B066201003NS1A sterile, hand-held manual surgical instrument designed to directly compress a blood vessel (ve
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