| Primary Device ID | 00888118146472 |
| NIH Device Record Key | bc7f745e-5e7a-4717-8979-36f03f0385b6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OTOBRADER |
| Version Model Number | 37-683-02-07 |
| 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 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 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 | 00888118146472 [Primary] |
| MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
[00888118146472]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-03 |
| Device Publish Date | 2025-05-26 |
| 00888118002440 | 00-102-40-07 |
| 00888118002433 | 00-102-39-07 |
| 00888118146472 | DINGMAN, LEFT |
| 00888118146465 | DINGMAN, RIGHT |