RapidVac

GUDID 10884524001449

Interlink Cable

Covidien LP

Electrical-only medical device connection cable, reusable
Primary Device ID10884524001449
NIH Device Record Key314bfb4c-8e05-437c-a570-970303e33158
Commercial Distribution StatusIn Commercial Distribution
Brand NameRapidVac
Version Model NumberSEA3730
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 Datetrue
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

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry

Device Identifiers

Device Issuing AgencyDevice ID
GS110884524001449 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FYDAPPARATUS, EXHAUST, SURGICAL

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-04-20
Device Publish Date2016-09-24

On-Brand Devices [RapidVac]

10884524000886Smoke Sponge Guard Tubing
10884524000879Smoke Tubing
10884524000329Smoke Tubing
20884524001071Smoke Wand
10884521134140Smoke Evacuator 110V
10884524001753Smoke Evacuator,220-240 V, 50/60 Hz; 8 Amps
10884524001449Interlink Cable
20884524001422ULPA Filter
10884524000893Footswitch
20884524001439Smoke Lap Tubing Kit with Valve
10884524001555Smoke Evacuator,100-120 V, 50/60 Hz; 10 Amps
10884521189669Remote Switch Activator

Trademark Results [RapidVac]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RAPIDVAC
RAPIDVAC
75442930 2360656 Live/Registered
COVIDIEN AG
1998-03-02

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