L1 RECONGUIDE

GUDID 00888118123978

KLS-Martin L.P.

Surgical instrument/implant rack
Primary Device ID00888118123978
NIH Device Record Keyfa95c47b-e2cc-448d-bad8-d26f01cb0a52
Commercial Distribution StatusIn Commercial Distribution
Brand NameL1 RECONGUIDE
Version Model Number55-990-53-04
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 Usefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100888118123978 [Primary]

FDA Product Code

FSMTRAY, SURGICAL, INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


[00888118123978]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-29
Device Publish Date2020-06-19

On-Brand Devices [L1 RECONGUIDE]

0088811812394725-500-35-07
0088811812393025-407-10-04
0088811812392325-500-33-07
0088811812391625-500-32-07
0088811812390925-500-31-07
0088811812389325-500-30-07
0088811812388625-500-29-07
0088811812387925-500-28-07
0088811812386225-500-27-07
0088811812385525-500-26-07
0088811812384825-500-25-07
0088811812383125-500-24-07
0088811812382425-500-23-07
0088811812381725-500-22-07
0088811812380025-500-21-07
0088811812379425-500-07-07
0088811812378725-500-06-07
0088811812377025-500-05-07
0088811812376325-500-04-07
0088811812375625-500-03-07
0088811812374925-500-02-07
0088811812373225-500-01-07
0088811812209425-500-20-07
0088811812208725-500-00-07
0088811812397855-990-53-04
0088811812396155-990-52-04
0088811812395455-990-51-04
00888118128119DRILL GUIDE, 2.0 MM, W/HANDLE
00888118128102HANDLE, SCREWDRIVER, FLAT, BLACK, 2.0/2.3 MM SCREW

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