| Primary Device ID | 00888118141989 |
| NIH Device Record Key | 0f020d65-2f97-4f84-9df9-6c6fa394a976 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | L1 |
| Version Model Number | CTM-01-2101-201 |
| 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 |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888118141989 [Primary] |
| FSM | TRAY, SURGICAL, INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
[00888118141989]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-08-26 |
| Device Publish Date | 2024-08-16 |
| 00888118086211 | 55-910-59-04 |
| 00888118136275 | CTM-01-2101-204 |
| 00888118136268 | CTM-01-2101-202 |
| 00888118136251 | CTM-01-2101-200 |
| 00888118136244 | CTM-01-2101-304 |
| 00888118136237 | CTM-01-2101-302 |
| 00888118136220 | CTM-01-2101-300 |
| 00888118139924 | CADDY, CTM-01-2106-101 AND CTM-01-2106-102, PACKAGE INCLUDES: 00888118139931 AND 00888118139948 |
| 00888118142085 | CTM-01-2101-802 |
| 00888118142078 | CTM-01-2101-801 |
| 00888118142061 | CTM-01-2101-800 |
| 00888118142054 | CTM-01-2101-702 |
| 00888118142047 | CTM-01-2101-701 |
| 00888118142030 | CTM-01-2101-700 |
| 00888118142023 | CTM-01-2101-602 |
| 00888118142016 | CTM-01-2101-601 |
| 00888118142009 | CTM-01-2101-600 |
| 00888118141996 | CTM-01-2101-301 |
| 00888118141989 | BASE, SCREW |
| 00888118139948 | LID, BLADE |
| 00888118139931 | BASE, BLADE |