| Primary Device ID | 05030267100989 |
| NIH Device Record Key | d39ef2d9-fe2a-4b1f-a27c-079cbf1f357a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CONNECTOR 10M - 22F. ONLY FOR USE WITH INTERSURGICAL 10MM FLEXTUBE |
| Version Model Number | 1660000 |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05030267054626 [Primary] |
| GS1 | 05030267100989 [Package] Contains: 05030267054626 Package: [40 Units] In Commercial Distribution |
| GS1 | 05030267100996 [Package] Contains: 05030267054626 Package: [160 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 | 2024-02-01 |
| Device Publish Date | 2024-01-24 |