Acetabular Insert Impactor

GUDID 00819251020725

Acetabular Insert Impactor, 36mm

TOTAL JOINT ORTHOPEDICS, INC.

Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable

Primary Device ID	00819251020725
NIH Device Record Key	4534d538-ebb9-4ace-89c2-427c58e26fe8
Commercial Distribution Status	In Commercial Distribution
Brand Name	Acetabular Insert Impactor
Version Model Number	1205.36.000
Company DUNS	078416717
Company Name	TOTAL JOINT ORTHOPEDICS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
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(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com
Phone	+1(801)486-6070
Email	udi@tjoinc.com

Device Dimensions

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Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0

Operating and Storage Conditions

Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, Specify	Between 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00819251020725 [Primary]

FDA Product Code

LXH	Orthopedic Manual Surgical Instrument