Lapro-Clip 8886848701

GUDID 10884521201941

Reusable Long Clip Applier

Covidien LP

Open-surgery ligation clip applier
Primary Device ID10884521201941
NIH Device Record Key89c34f75-7f90-4821-a541-ccbbe4eebc87
Commercial Distribution StatusIn Commercial Distribution
Brand NameLapro-Clip
Version Model Number8886848701
Catalog Number8886848701
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
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
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

Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0
Length10 Millimeter
Device Size Text, specify0

Operating and Storage Conditions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS110884521201941 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

[10884521201941]

Moist Heat or Steam Sterilization


[10884521201941]

Moist Heat or Steam Sterilization


[10884521201941]

Moist Heat or Steam Sterilization


[10884521201941]

Moist Heat or Steam Sterilization


[10884521201941]

Moist Heat or Steam Sterilization


[10884521201941]

Moist Heat or Steam Sterilization


[10884521201941]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-09-23
Device Publish Date2016-09-24

On-Brand Devices [Lapro-Clip]

20884521057651Absorbable Ligating Clip Cartridge
20884521057644Absorbable Ligating Clip Cartridge
10884521201941Reusable Long Clip Applier
20884521208466Absorbable Ligating Clip Cartridge
10884521057586Reusable Clip Applier
10884521208438Absorbable Ligating Clip Cartridge
20884521057699Absorbable Ligating 8 Clip Cartridge
20884521057675Absorbable Ligating Clip Cartridge
20884521057668Absorbable Ligating Clip Cartridge
10884521057630Reusable Clip Applier
10884521057623Reusable Clip Applier
10884521057616Reusable Clip Remover

Trademark Results [Lapro-Clip]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LAPRO-CLIP
LAPRO-CLIP
74331487 1870450 Live/Registered
COVIDIEN AG
1992-11-16

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