| Primary Device ID | 05030267005185 |
| NIH Device Record Key | e70222f3-31fc-4b8e-902b-7ac25dc31957 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | T-PIECE, 22M, 22M/15F, 22M, WITH ONE-WAY VALVES |
| Version Model Number | 1954000 |
| 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 | 05030267005185 [Package] Contains: 05030267057207 Package: [25 Units] In Commercial Distribution |
| GS1 | 05030267005192 [Package] Contains: 05030267057207 Package: [100 Units] In Commercial Distribution |
| GS1 | 05030267057207 [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 | 2023-06-23 |
| Device Publish Date | 2023-06-15 |