| Primary Device ID | 00888118120113 |
| NIH Device Record Key | 19a70818-a309-4555-bda1-c6df06d9de06 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCISSORS |
| Version Model Number | 24-850-23-07 |
| 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 |
| 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 | 00888118120113 [Primary] |
| HAO | INSTRUMENT, SURGICAL, NON-POWERED |
| LRW | SCISSORS, GENERAL, SURGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
[00888118120113]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-08-21 |
| Device Publish Date | 2018-11-22 |