| Primary Device ID | 00810055472130 |
| NIH Device Record Key | 2829bdf2-030b-447b-a7f9-c4236892ce50 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Instrumentarium |
| Version Model Number | s.50.440 |
| Company DUNS | 203088166 |
| Company Name | Société Chirurgicale Instrumentarium Inc |
| 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810055472130 [Primary] |
| KTG | Knife, Ent |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
[00810055472130]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-19 |
| Device Publish Date | 2021-08-11 |