HeartSpan® FND-020-06/A

GUDID 10884450451707

Merit Medical

Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use Cardiac transseptal needle, single-use
Primary Device ID10884450451707
NIH Device Record Keyb67afbd9-d3f3-4fe7-ad2a-e13433da8673
Commercial Distribution StatusIn Commercial Distribution
Brand NameHeartSpan®
Version Model Number00884450451700
Catalog NumberFND-020-06/A
Company DUNS065673912
Company NameMerit Medical
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 Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS100884450451700 [Primary]
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution
GS110884450451707 [Package]
Contains: 00884450451700
Package: [5 Units]
In Commercial Distribution

FDA Product Code

DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar
DRCTrocar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-14
Device Publish Date2020-09-04

On-Brand Devices [HeartSpan®]

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1088445016913800884450169131
0088445016912400884450169124
1088445016911400884450169117
1088445016907700884450169070

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