| Primary Device ID | 08809265158790 |
| NIH Device Record Key | 4c456e1d-0cd2-4219-aec1-629a820498db |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Surgical Instrument |
| Version Model Number | 111-026-1 |
| Company DUNS | 688811603 |
| Company Name | Jeil Medical Corporation |
| 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 | true |
| 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 | 08809265158790 [Primary] |
| GEA | Cannula, Surgical, General & Plastic Surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
[08809265158790]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2024-04-26 |
| Device Publish Date | 2018-09-06 |