AV8571

GUDID 20845854053079

SECONDARY ARM WITH KEYBOARD TRAY

Conmed Corporation

Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack Medical device integration rack
Primary Device ID20845854053079
NIH Device Record Key84307b25-dd54-49af-8a78-26370578a841
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberAV8571
Catalog NumberAV8571
Company DUNS071595540
Company NameConmed Corporation
Device Count1
DM Exempttrue
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(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

Device Identifiers

Device Issuing AgencyDevice ID
GS120845854053079 [Primary]

FDA Product Code

KQMCAMERA, SURGICAL AND ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-31
Device Publish Date2020-07-23

Devices Manufactured by Conmed Corporation

20653405007194 - UltraClean2024-04-18 UltraClean Accessory Electrode 1" Coated Blade with Extended Insulation
10845854026793 - GENESYS CROSSFT2024-04-18 5.5MM CROSSFT-BC ANCHOR, W/DISP, TRP
10845854026809 - GENESYS CROSSFT2024-04-18 6.5MM CROSSFT-BC ANCHOR, W/DISP, DBL
10845854026816 - GENESYS CROSSFT2024-04-18 6.5MM CROSSFT-BC ANCHOR, W/DISP, TRP
10845854027868 - GENESYS PRESSFT2024-04-18 GENESYS PRESS FT 2.1 W/ONE # 2 (5 METRIC) HI-FI SUTURE, HIP
10845854027899 - GENESYS PRESSFT2024-04-18 GENSESYS PRESSFT 2.6 W/ ONE # 2 (5 METRIC) HI-FI- SUTURE, HIP
10845854034606 - GENESYS CROSSFT2024-04-18 GENESYS CROSSFT 5.5MM SUTURES ANCHOR, W/ 3 HI-FI #2 (5 METRIC) SUTURES W/NEEDLES
10845854034613 - GENESYS CROSSFT2024-04-18 GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 2 HI-FI (5 METRIC) SUTURES W/NEEDLES
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