GRAFTMAX KS-IND

GUDID 10845854042731

GraftMax™ Indicator

Conmed Corporation

General external orthopaedic fixation system implantation kit, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable

Primary Device ID	10845854042731
NIH Device Record Key	bf0257cb-fef4-41ec-a46a-a35c2715b58d
Commercial Distribution Status	In Commercial Distribution
Brand Name	GRAFTMAX
Version Model Number	KS-IND
Catalog Number	KS-IND
Company DUNS	071595540
Company Name	Conmed Corporation
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com
Phone	+1(866)426-6633
Email	CustomerExperience@conmed.com

Operating and Storage Conditions

Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY
Special Storage Condition, Specify	Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854042731 [Primary]
GS1	20845854042738 [Direct Marking]

FDA Product Code

GFG	BIT, SURGICAL