HeartSpan® FND-025-02/A

GUDID 00884450451724

Merit Medical Systems, Inc.

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 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 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 ID00884450451724
NIH Device Record Keyc7f9054a-61ac-4927-aecd-9adde162d0fd
Commercial Distribution StatusIn Commercial Distribution
Brand NameHeartSpan®
Version Model Number00884450451724
Catalog NumberFND-025-02/A
Company DUNS184763290
Company NameMerit Medical Systems, Inc.
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100884450451724 [Primary]

FDA Product Code

DRCTrocar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-09
Device Publish Date2020-10-30

On-Brand Devices [HeartSpan®]

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0088445069370400884450693704
00884450693711C
0088445046600100884450466001

Trademark Results [HeartSpan]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HEARTSPAN
HEARTSPAN
87043746 5064437 Live/Registered
Merit Medical Systems, Inc.
2016-05-19
HEARTSPAN
HEARTSPAN
77169337 3680277 Dead/Cancelled
Thomas Medical Products, Inc.
2007-04-30

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