| Primary Device ID | 05030267005017 |
| NIH Device Record Key | db1ad2f0-1d43-4ffc-91c7-2fba6fc62d03 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CONNECTOR, 22M, 22M WITH ONE-WAY VALVE |
| Version Model Number | 1950000 |
| Company DUNS | 785952607 |
| Company Name | INTERSURGICAL INCORPORATED |
| 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 | 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 | 05030267005000 [Package] Contains: 05030267057085 Package: [40 Units] In Commercial Distribution |
| GS1 | 05030267005017 [Package] Contains: 05030267057085 Package: [160 Units] In Commercial Distribution |
| GS1 | 05030267057085 [Primary] |
| 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 | 2021-10-13 |
| Device Publish Date | 2021-10-05 |
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