| Primary Device ID | 00888118143389 |
| NIH Device Record Key | b4f3613a-be0d-477b-8574-ca6ba9c90154 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LEVEL ONE CMF |
| Version Model Number | 50-330-08-09 |
| Company DUNS | 826499238 |
| Company Name | KLS-Martin L.P. |
| 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 |
| 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 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888118143389 [Primary] |
| JEY | PLATE, BONE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
[00888118143389]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-10-02 |
| Device Publish Date | 2025-09-24 |
| 10888118113921 | SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V |
| 10888118113914 | SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V |
| 10888118113907 | SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V |
| 10888118113891 | SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V |
| 10888118113884 | SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V |
| 10888118113877 | SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V |
| 10888118113617 | SCREW, ONEDRIVE, DRILL FREE, TI-6AL-4V |
| 10888118113600 | SCREW, ONEDRIVE, DRILL FREE, TI-6AL-4V |
| 10888118113549 | SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, 46* FLUTE, STAINLESS STEEL ASTM F138 |
| 10888118113532 | SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, 46* FLUTE, STAINLESS STEEL ASTM F138 |
| 10888118102215 | SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, STAINLESS STEEL ASTM F138 |
| 10888118102208 | SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, STAINLESS STEEL ASTM F138 |
| 10888118095371 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118095364 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118095357 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118095340 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118095333 | SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V |
| 10888118095326 | SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V |
| 10888118095319 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118095302 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118095296 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118094619 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118094602 | SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V |
| 10888118094589 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118094565 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118094558 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118094541 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118094534 | SCREW, MAXDRIVE, F3, TI-6AL-4V |
| 10888118094527 | SCREW, MAXDRIVE, FLAT TIP, TI-6AL-4V |
| 10888118094510 | SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118094503 | SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118094497 | SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118094480 | SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118094473 | SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118094466 | SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118094459 | SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118073553 | SCREW, CROSSDRIVE, TLTS, FASTENING, TEMPORARY CONDYLAR IMPLANT, TI-6AL-4V |
| 10888118073492 | SCREW, CROSSDRIVE, TLCK, FASTENING, TEMPORARY CONDYLAR IMPLANT, TI-6AL-4V |
| 10888118048728 | SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118048704 | SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118048681 | SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118048667 | SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V |
| 10888118048643 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118048629 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118048605 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118048582 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118048568 | SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V |
| 10888118048544 | SCREW, MAXDRIVE, TLTS, TI-6AL-4V |
| 10888118048520 | SCREW, MAXDRIVE, TLTS, TI-6AL-4V |
| 10888118048506 | SCREW, MAXDRIVE, TLTS, TI-6AL-4V |