ClosureFast

GUDID 10884521140417

Tumescent Pump Foot Pedal,Gradual Control

Covidien LP

Laboratory liquid dispenser, electronic
Primary Device ID10884521140417
NIH Device Record Key9335f3df-b6b2-4675-aaa4-233e36a4ceaa
Commercial Distribution Discontinuation2016-09-24
Commercial Distribution StatusNot in Commercial Distribution
Brand NameClosureFast
Version Model NumberTPED-G
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 Numbertrue
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(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 Identifiers

Device Issuing AgencyDevice ID
GS110884521140417 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRNPump, infusion

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-09-19
Device Publish Date2016-09-24

On-Brand Devices [ClosureFast]

10884521181816Procedure Pack
10884521174924Endovenous Radiofrequency Ablation (RFA) Catheter,3 cm Heating Element,7 Fr/Ch (2.3 mm) x 60 cm
10884521058071Endovenous Radiofrequency Ablation (RFA) Catheter,7 cm Heating Element,7 Fr/Ch (2.3 mm) x 60 cm
10884521058057Endovenous Radiofrequency Ablation (RFA) Catheter,7 cm Heating Element,7 Fr/Ch (2.3 mm) x 100 cm
20884521140353Micro Introducer Sheath Set
20884521140308Introducer Sheath Set
20884521173528Introducer Sheath Set
20884521140292Micro Introducer Sheath Set
20884521592626Guidewire Single Ended, SS, Fixed Core
20884521058122Ultrasound Probe Cover,6"" x 96"" (15.2 cm x 2.4 m)
20884521140407Tumescent Infiltration Kit
20884521140384Micro Puncture Kit
20884521140377Micro Puncture Kit
10884521140417Tumescent Pump Foot Pedal,Gradual Control
20884521140223Guidewire,Single Ended, PTFE, Fixed Core,0.018"" (0.46 mm) x 45 cm
10884521140424Tumescent Pump Foot Pedal,On/Off Control
20884521173511Arterial Needle,Echogenic Tip,21 G (0.813 mm) x 2.75"" (70 mm)
20884521140261Guidewire,Double Ended, PTFE, Fixed Core,0.035"" (0.89 mm) x 45 cm
20884521140254Guidewire,J Tip, PTFE, Fixed Core,0.025"" (0.64 mm) x 260 cm
20884521140247Guidewire,Double Ended, PTFE, Fixed Core,0.025"" (0.64 mm) x 150 cm
20884521140193Arterial Needle,21 G (0.813 mm) x 2.75"" (70 mm)
20884521140186Arterial Needle,Ultra Thin Wall with Echogenic Tip,19 G (1.067 mm) x 2.75"" (70 mm)
20884521140179Arterial Needle,Ultra Thin Wall,19 G (1.067 mm) x 2.75"" (70 mm)
20884521140209Compression Bandages,Cohesive,4"" x 15' (10.16 cm x 4.572 m)
20884521140216Compression Bandages,Cohesive,6"" x 15' (15.24 cm x 4.572 m)

Trademark Results [ClosureFast]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CLOSUREFAST
CLOSUREFAST
78981195 3738306 Live/Registered
COVIDIEN LP
2005-11-15
CLOSUREFAST
CLOSUREFAST
78754633 not registered Dead/Abandoned
VNUS Medical Technologies, Inc.
2005-11-15

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