LEVEL ONE CMF

GUDID 00888118131379

PLATE, ORTHOG, GENIOPLASTY, X SHP, W/TAB, 2.0 MM SCREW, CP TITANIUM

KLS-Martin L.P.

Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized
Primary Device ID00888118131379
NIH Device Record Keyc2c64e88-a13b-4e16-b650-21c164925a26
Commercial Distribution StatusIn Commercial Distribution
Brand NameLEVEL ONE CMF
Version Model Number50-305-32-09
Company DUNS826499238
Company NameKLS-Martin L.P.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100888118131379 [Primary]

FDA Product Code

JEYPLATE, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


[00888118131379]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-02
Device Publish Date2022-02-22

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10888118095333SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V
10888118095326SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V
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10888118094589SCREW, MAXDRIVE, F3, TI-6AL-4V
10888118094565SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
10888118094558SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
10888118094541SCREW, MAXDRIVE, F3, TI-6AL-4V
10888118094534SCREW, MAXDRIVE, F3, TI-6AL-4V
10888118094527SCREW, MAXDRIVE, FLAT TIP, TI-6AL-4V
10888118094510SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118094503SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118094497SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118094480SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118094473SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118094466SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118094459SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118073553SCREW, CROSSDRIVE, TLTS, FASTENING, TEMPORARY CONDYLAR IMPLANT, TI-6AL-4V
10888118073492SCREW, CROSSDRIVE, TLCK, FASTENING, TEMPORARY CONDYLAR IMPLANT, TI-6AL-4V
10888118048728SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V
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10888118048681SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118048667SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V
10888118048643SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
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10888118048605SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
10888118048582SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
10888118048568SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
10888118048544SCREW, MAXDRIVE, TLTS, TI-6AL-4V
10888118048520SCREW, MAXDRIVE, TLTS, TI-6AL-4V
10888118048506SCREW, MAXDRIVE, TLTS, TI-6AL-4V

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