| Primary Device ID | 00816472023696 |
| NIH Device Record Key | 95b928ff-f0dd-4e70-a0cf-5987cbff1fcc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Multipac Anesthesia Breathing Circuit |
| Version Model Number | M5782002 |
| 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 | 00816472023689 [Primary] |
| GS1 | 00816472023696 [Package] Contains: 00816472023689 Package: [10 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 | 2022-12-21 |
| 00816472022477 | Multipac Anesthesia breathing circuit |
| 00816472023696 | Multipac Anesthesia Breathing Circuit |