22.7005

GUDID 20845854037710

2.75 X 90MM SMALL JOINT OPEN CURETTE

Conmed Corporation

Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable
Primary Device ID20845854037710
NIH Device Record Key06d590d1-2dda-4b19-9c23-64f93f2d5576
Commercial Distribution StatusIn Commercial Distribution
Version Model Number22.7005
Catalog Number22.7005
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 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(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

Device Dimensions

Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854037713 [Primary]
GS120845854037710 [Direct Marking]

FDA Product Code

MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


[20845854037710]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-07-15
Device Publish Date2020-09-24

Devices Manufactured by Conmed Corporation

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30845854026803 - GENESYS CrossFT, Hi-Fi2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Two #2 (5 metric) Hi-Fi Sutures
30845854026810 - GENESYS CrossFT, Hi-Fi2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures
30845854027862 - GENESYS PressFT, Hi-Fi2024-04-25 GENESYS PressFT 2.1 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
30845854027893 - GENESYS PressFT, Hi-Fi2024-04-25 GENESYS PressFT 2.6 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
30845854034600 - GENESYS CrossFT, Hi-Fi2024-04-25 GENESYS CrossFT 5.5 mm Suture Anchor, w/3 Hi-Fi #2 (5 metric) Sutures w/Needles
30845854034617 - GENESYS CrossFT, Hi-Fi2024-04-25 GENESYS CrossFT 6.5 mm Suture Anchor, w/2 Hi-Fi #2 (5 metric) Sutures w/Needles
30653405988643 - Argo Knotless GENESYS2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor

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