| Primary Device ID | 05030267139156 |
| NIH Device Record Key | 40fb4dec-e6ff-48aa-9571-4ba9cbb59368 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SWIVEL CONNECTOR 22M - 22M/15F |
| Version Model Number | 5802801 |
| Company DUNS | 785952607 |
| Company Name | Intersurgical Incorporated |
| 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 | true |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05030267139132 [Primary] |
| GS1 | 05030267139149 [Package] Contains: 05030267139132 Package: [300 Units] In Commercial Distribution |
| GS1 | 05030267139156 [Package] Contains: 05030267139132 Package: [150 Units] In Commercial Distribution |
| BZA | Connector, Airway (Extension) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-23 |
| Device Publish Date | 2023-06-15 |