Aortic Cutter 4.3MM AC-3043

GUDID 00607567700271

Aortic Cutter 4.3MM

MAQUET CARDIOVASCULAR LLC

Aorta punch, single-use Aorta punch, single-use Aorta punch, single-use
Primary Device ID00607567700271
NIH Device Record Key593d03b4-3675-4b9a-9033-198a5d84b5a6
Commercial Distribution StatusIn Commercial Distribution
Brand NameAortic Cutter 4.3MM
Version Model NumberAC-3043
Catalog NumberAC-3043
Company DUNS022348156
Company NameMAQUET CARDIOVASCULAR LLC
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone888-880-2874
Emailcssurgery@maquet.com
Phone888-880-2874
Emailcssurgery@maquet.com
Phone888-880-2874
Emailcssurgery@maquet.com

Device Dimensions

Outer Diameter4.3 Millimeter
Outer Diameter4.3 Millimeter
Outer Diameter4.3 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100607567700271 [Package]
Contains: 00607567700277
Package: 5 pack box [5 Units]
Discontinued: 2018-05-29
Not in Commercial Distribution
GS100607567700277 [Primary]
GS120607567700271 [Package]
Contains: 00607567700277
Package: 5 pack box [5 Units]
In Commercial Distribution

FDA Product Code

FZTCutter, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-05-30
Device Publish Date2016-09-24

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