Infinity AIM™ KSC20

GUDID 20845854649913

Infinity AIM™ Suture Cutter and Skid

Conmed Corporation

Suture cutter, single-use Suture cutter, single-use Suture cutter, single-use Suture cutter, single-use Suture cutter, single-use Suture cutter, single-use Suture cutter, single-use
Primary Device ID20845854649913
NIH Device Record Key9ea268aa-6cf8-47cd-9774-4ccc551c1334
Commercial Distribution StatusIn Commercial Distribution
Brand NameInfinity AIM™
Version Model NumberKSC20
Catalog NumberKSC20
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 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(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
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
GS120845854649913 [Primary]

FDA Product Code

LXHOrthopedic manual surgical instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-06-23
Device Publish Date2022-06-15

Devices Manufactured by Conmed Corporation

20653405012006 - EXCEL2024-03-27 EXCEL 10FT (3.05M) INSUFFLATION TUBING SET WITH 0.1 MICRON FILTER
20653405012013 - EXCEL2024-03-27 EXCEL 10FT (3.05M) INSUFFLATION TUBING SET WITH 0.1 MICRON FILTER
10653405040750 - CONMED2024-03-27 EQUIPMENT CART ELECTROSURGICAL UNIT CART
10653405054870 - SYSTEM 24502024-03-27 SYSTEM 2450 STACKING ADAPTER
20845854013233 - ENTREE2024-03-26 LIGHT GUIDE FITTING FOR STORZ, AND LINVATEC LIGHT SOURCES
20845854016692 - CONMED2024-03-26 10MM X 110MM ENTREE II CANNULA, REUSABLE
20845854038540 - CONMED2024-03-26 LIGHT GUIDE FITTING FOR A.C.M.I STYLE SCOPES
20845854038557 - CONMED2024-03-26 LIGHT GUIDE FITTING FOR WOLF AND DYONICS LIGHT SOURCES

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