| Primary Device ID | 00810130204083 |
| NIH Device Record Key | 67eb0056-8d0e-430d-ac8d-dfd0249bd365 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MSI |
| Version Model Number | 40.9215 |
| Company DUNS | 118447158 |
| Company Name | Modern Surgical Instruments LLC |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810130204083 [Primary] |
| GAD | Retractor |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
[00810130204083]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-25 |
| Device Publish Date | 2024-06-17 |