Primary Device ID | 00888118089120 |
NIH Device Record Key | 158c6bfe-402d-4ebe-ba55-929680497334 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BLOCK, STERILE |
Version Model Number | 55-969-91-71 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888118089120 [Primary] |
JXS | BLOCK, CUTTING, ENT, STERILE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-08-23 |
Device Publish Date | 2018-09-26 |
00888118143204 - LEVEL ONE THORACIC, STERILE | 2025-04-30 SCREW GUIDE, STERNAL, LADDER |
00888118143211 - LEVEL ONE THORACIC, STERILE | 2025-04-30 SCREW GUIDE, STERNAL, X SHAPE |
00888118145086 - IPS | 2025-04-30 IMPLANT, MIDFACE, W/AUGMENTATION, SMALL, LP, TI-6AL-4V |
00888118145093 - IPS | 2025-04-30 IMPLANT, MIDFACE, W/AUGMENTATION, MEDIUM, LP, TI-6AL-4V |
00888118145109 - IPS | 2025-04-30 IMPLANT, MIDFACE, W/AUGMENTATION, LARGE, LP, TI-6AL-4V |
00888118145529 - IPS | 2025-04-30 SUPPLEMENTAL MODEL, HALF, MICROTIA, LP |
00888118145536 - IPS | 2025-04-30 MARKING GUIDE, MICROTIA, POSITIONING, LP |
00888118145543 - IPS | 2025-04-30 MARKING GUIDE, W/PLANNING, MICROTIA, POSITIONING, LP |