PLUMEPEN PROTIP520

GUDID 40845854061320

PlumePen Pro Disposable Capture Port Tips 5 in (12.7 cm)

Conmed Corporation

Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use
Primary Device ID40845854061320
NIH Device Record Keye8111412-9656-403a-b321-cf6516c899da
Commercial Distribution Discontinuation2023-09-12
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePLUMEPEN
Version Model NumberPROTIP520
Catalog NumberPROTIP520
Company DUNS071595540
Company NameConmed Corporation
Device Count20
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(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.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
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
GS100845854061322 [Unit of Use]
GS120845854061326 [Primary]
GS140845854061320 [Package]
Contains: 20845854061326
Package: Box [20 Units]
Discontinued: 2023-09-12
Not in Commercial Distribution

FDA Product Code

GEIElectrosurgical, cutting & coagulation & accessories

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


[40845854061320]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-09-13
Device Publish Date2020-06-06

On-Brand Devices [PLUMEPEN]

20845854061296PLP2501
40845854061320PlumePen Pro Disposable Capture Port Tips 5 in (12.7 cm)
00845854084246PlumePen Pro, 10ft, PTFE, Non-Sterile, 20/BOX
00845854084239PlumePen Pro, 15ft, PTFE, Non-Sterile, 20/BOX
00845854084222PlumePen Ultra, 10ft, PTFE, Non-Sterile, 20/BOX
00845854084215PlumePen Ultra, 15ft, PTFE, Non-Sterile, 20/BOX
00845854084208PlumePen Elite, 10ft, SS, Non-Sterile, 20/BOX
00845854084192PlumePen Elite, 10ft, PTFE, Non-Sterile, 20/BOX
00845854084185PlumePen Elite, 15ft, PTFE, Non-Sterile, 20/BOX
00845854061308PLP2520
00845854061261PLP1020
40845854061337PlumePen Pro Disposable Capture Port Tips 6 in (15.24 cm)
40845854061313PlumePen Pro Disposable Capture Port Tips 4 in (10.16 cm)

Trademark Results [PLUMEPEN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PLUMEPEN
PLUMEPEN
85076204 4376795 Live/Registered
Medtek Devices, Inc.
2010-07-01

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