| Primary Device ID | 08800089416691 |
| NIH Device Record Key | 8105705f-ba20-44be-a709-c0ac4c5e4104 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | INLET System Surgical Instrument |
| Version Model Number | IN112-129 |
| Company DUNS | 688811603 |
| Company Name | Jeil Medical Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | 08800089416691 [Primary] |
| KCT | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
[08800089416691]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-04-04 |
| Device Publish Date | 2021-11-18 |