| Primary Device ID | 00816472022538 | 
| NIH Device Record Key | 128a3d0b-7555-4d18-9ebf-6b18f07f4189 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Multipac® Anesthesia Breathing System | 
| Version Model Number | M5704000 | 
| 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 | 00816472022521 [Primary] | 
| GS1 | 00816472022538 [Package] Contains: 00816472022521 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 | 2023-01-10 | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() MULTIPAC  79117558  4281314 Live/Registered  | 
        SICK AG  2012-06-15  | 
![]() MULTIPAC  75252144  2135876 Live/Registered  | 
        Intersurgical Incorporated  1997-03-05  | 
![]() MULTIPAC  74647955  2009529 Live/Registered  | 
        PENTAIR TECHNICAL SOLUTIONS GMBH  1995-03-17  | 
![]() MULTIPAC  73707740  1527901 Dead/Cancelled  | 
        MERLIN GERIN, S.A.  1988-01-26  | 
![]() MULTIPAC  73671570  1478459 Dead/Cancelled  | 
        WATKINS-JOHNSON COMPANY  1987-07-13  |