C3278

GUDID 10845854016688

Autoclavable Non-Transparent Light Guide 5mm x 3m

Conmed Corporation

Fibreoptic light cable
Primary Device ID10845854016688
NIH Device Record Key24590f7a-d86c-4b02-9204-612f128b814f
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberC3278
Catalog NumberC3278
Company DUNS071595540
Company NameConmed Corporation
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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(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
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
GS110845854016688 [Primary]

FDA Product Code

EQHSOURCE, CARRIER, FIBEROPTIC LIGHT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


[10845854016688]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-06
Device Publish Date2020-04-28

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10653405990741 - Hall® Titan™2026-01-06 Hall® Titan™ XE Dual Trigger Battery Handpiece
30653405990714 - Infinity2025-12-09 Infinity Retro-Reamer, 10.5 mm

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