| Primary Device ID | 00816472020558 |
| NIH Device Record Key | 0cc9c971-666c-4222-9772-9883d146f47a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Breathing Circuit |
| Version Model Number | A0066000 |
| Company DUNS | 785952607 |
| Company Name | Intersurgical Incorporated |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | 00816472020541 [Primary] |
| GS1 | 00816472020558 [Package] Contains: 00816472020541 Package: [15 Units] In Commercial Distribution |
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2025-02-11 |
| Device Publish Date | 2023-01-12 |
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