| Primary Device ID | 00816472020930 |
| NIH Device Record Key | e77705f9-7c78-4533-bb37-cb67c8eae620 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Convenience Pack |
| Version Model Number | J0004001 |
| 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 | 00816472020923 [Primary] |
| GS1 | 00816472020930 [Package] Contains: 00816472020923 Package: [20 Units] In Commercial Distribution |
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-21 |
| Device Publish Date | 2023-06-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CONVENIENCE PACK 76302518 not registered Dead/Abandoned |
Choice One Communications, Inc. 2001-08-21 |
![]() CONVENIENCE PACK 73597079 1435144 Dead/Cancelled |
AMERICAN SEED CORPORATION 1986-05-05 |
![]() CONVENIENCE PACK 73506663 1350132 Live/Registered |
SUNBELT MANUFACTURING, INC. 1984-11-01 |