LEVEL ONE, STERILE

GUDID 00888118106063

KLS-Martin L.P.

Orthopaedic bone-fragment manipulator, single-use, sterile Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use Orthopaedic bone-fragment manipulator, single-use
Primary Device ID00888118106063
NIH Device Record Keyc50424a0-d399-4d4d-b86c-f0c05224f1c1
Commercial Distribution StatusIn Commercial Distribution
Brand NameLEVEL ONE, STERILE
Version Model Number24-015-67-71
Company DUNS826499238
Company NameKLS-Martin L.P.
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(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
Phone+1(904)641-7746
EmailKLS-UDI-Info@klsmartin.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100888118106063 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-03-09
Device Publish Date2018-09-27

On-Brand Devices [LEVEL ONE, STERILE]

0088811809691350-997-19-71
0088811809689050-997-07-71
0088811809687650-997-05-71
0088811809685250-996-17-71
0088811809683850-996-15-71
0088811809681450-996-13-71
0088811809679150-996-11-71
0088811809677750-996-09-71
0088811809675350-996-07-71
0088811809673950-996-05-71
0088811809671550-995-17-71
0088811809669250-995-07-71
0088811809667850-995-05-71
0088811805438826-975-45-71
0088811805437126-975-44-71
0088811805413526-475-20-71
0088811805408126-475-10-71
0088811805399226-460-20-71
0088811805394726-460-10-71
0088811805337426-158-23-71
0088811805335026-158-20-71
0088811805333626-158-18-71
0088811805331226-158-16-71
0088811805329926-158-15-71
0088811805327526-158-12-71
0088811805325126-158-11-71
0088811805323726-158-10-71
0088811805300826-153-23-71
0088811805298826-153-20-71
0088811805296426-153-18-71
0088811805294026-153-16-71
0088811805292626-153-15-71
0088811805290226-153-11-71
0088811810606324-015-67-71
0088811812561350-022-15-71
0088811812560650-022-03-71
0088811812559025-457-05-71
0088811812558325-452-07-71
0088811812557625-452-05-71
0088811812556925-449-09-71
0088811812555225-449-07-71
0088811812554525-449-05-71
0088811812163925-469-11-71
0088811812162225-452-00-71
0088811812161525-449-16-71
0088811809665450-993-20-71
0088811809663050-993-15-71
0088811809661650-991-20-71
0088811809659350-991-15-71
0088811809568825-043-95-71

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