Ligature Sleeve LS21-10

GUDID 20885672008349

Ligature Sleeve

Oscor Inc.

Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead Endocardial defibrillation lead
Primary Device ID20885672008349
NIH Device Record Keyd8511877-694f-4f5a-a574-1d5fb1037024
Commercial Distribution StatusIn Commercial Distribution
Brand NameLigature Sleeve
Version Model Number664760-303
Catalog NumberLS21-10
Company DUNS101835833
Company NameOscor Inc.
Device Count10
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com
Phone+1(727)937-2511
Emailsales@oscor.com

Device Dimensions

Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter
Lumen/Inner Diameter2.1 Millimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100885672008345 [Unit of Use]
GS120885672008349 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DTBpermanent pacemaker Electrode

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 Date2017-11-18

On-Brand Devices [Ligature Sleeve]

70836559007424LS17B20
70836559002023LS26B20
70836559002016LS24B20
70836559002009LS21B20
70836559001996LS18B20
70836559001989LS15B20
20885672008349Ligature Sleeve
20802526563229664760-302
00836559007425LS-17
00836559002024LS-26
00836559002017LS-24
00836559002000LS-21
00836559001997LS-18
00836559001980LS-15

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