Argo Knotless GENESYS KBC475RSP

GUDID 10653405988601

4.75 mm Argo KnotlessTM GENESYSTM Reusable Smooth Punch

Conmed Corporation

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Primary Device ID10653405988601
NIH Device Record Key46c17ace-551f-46c9-af8a-eb8c3c713c6a
Commercial Distribution StatusIn Commercial Distribution
Brand NameArgo Knotless GENESYS
Version Model NumberKBC475RSP
Catalog NumberKBC475RSP
Company DUNS071595540
Company NameConmed Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY;DO NOT CRUSH

Device Identifiers

Device Issuing AgencyDevice ID
GS110653405988601 [Direct Marking]
GS130653405988605 [Primary]

FDA Product Code

LXHOrthopedic manual surgical instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


[10653405988601]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-22
Device Publish Date2024-04-12

On-Brand Devices [Argo Knotless GENESYS]

106534059886014.75 mm Argo KnotlessTM GENESYSTM Reusable Smooth Punch
106534059885955.5 mm Argo KnotlessTM GENESYSTM Reusable Tap
106534059885884.75 mm Argo KnotlessTM GENESYSTM Reusable Tap
106534059885714.75/5.5 mm Argo KnotlessTM GENESYSTM Reusable Broaching Punch
306534059887664.75/5.5 mm Argo KnotlessTM GENESYSTM Disposable Broaching Punch
306534059887594.75 mm Argo KnotlessTM GENESYSTM Disposable Smooth Punch
306534059887424.75 mm Argo KnotlessTM GENESYSTM Disposable Tap
306534059887355.5 mm Argo KnotlessTM GENESYSTM Disposable Tap
306534059886984.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black
306534059886814.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue
306534059886744.75mm Argo Knotless® GENESYSTM Anchor
306534059886675.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black
306534059886505.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue
306534059886435.5mm Argo Knotless® GENESYSTM Anchor

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