Primary Device ID | 00888118128119 |
NIH Device Record Key | f010b711-1696-4ee8-ab4b-3ac0afac00aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | L1 RECONGUIDE |
Version Model Number | 25-500-40-07 |
Company DUNS | 826499238 |
Company Name | KLS-Martin L.P. |
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 | 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 |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888118128119 [Primary] |
FZX | Guide, surgical, instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
[00888118128119]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-08-23 |
Device Publish Date | 2020-05-22 |
00888118123947 | 25-500-35-07 |
00888118123930 | 25-407-10-04 |
00888118123923 | 25-500-33-07 |
00888118123916 | 25-500-32-07 |
00888118123909 | 25-500-31-07 |
00888118123893 | 25-500-30-07 |
00888118123886 | 25-500-29-07 |
00888118123879 | 25-500-28-07 |
00888118123862 | 25-500-27-07 |
00888118123855 | 25-500-26-07 |
00888118123848 | 25-500-25-07 |
00888118123831 | 25-500-24-07 |
00888118123824 | 25-500-23-07 |
00888118123817 | 25-500-22-07 |
00888118123800 | 25-500-21-07 |
00888118123794 | 25-500-07-07 |
00888118123787 | 25-500-06-07 |
00888118123770 | 25-500-05-07 |
00888118123763 | 25-500-04-07 |
00888118123756 | 25-500-03-07 |
00888118123749 | 25-500-02-07 |
00888118123732 | 25-500-01-07 |
00888118122094 | 25-500-20-07 |
00888118122087 | 25-500-00-07 |
00888118123978 | 55-990-53-04 |
00888118123961 | 55-990-52-04 |
00888118123954 | 55-990-51-04 |
00888118128119 | DRILL GUIDE, 2.0 MM, W/HANDLE |
00888118128102 | HANDLE, SCREWDRIVER, FLAT, BLACK, 2.0/2.3 MM SCREW |