Purstring 020730

GUDID 20884521051475

Purse String Device

Covidien LP

Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device Suture retention device
Primary Device ID20884521051475
NIH Device Record Key35a5912a-028e-4265-bfba-bd217b3b2ba4
Commercial Distribution StatusIn Commercial Distribution
Brand NamePurstring
Version Model Number020730
Catalog Number020730
Company DUNS058614483
Company NameCovidien LP
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Device Dimensions

Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0
Length45 Millimeter
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;
Special Storage Condition, SpecifyBetween 0 and 0 *null;

Device Identifiers

Device Issuing AgencyDevice ID
GS110884521051478 [Primary]
GS120884521051475 [Package]
Contains: 10884521051478
Package: CASE [3 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-09-15
Device Publish Date2018-08-10

On-Brand Devices [Purstring]

20884521051475Purse String Device
20884521051437Purse String Device

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