| Primary Device ID | 00815849023482 |
| NIH Device Record Key | 8894bca9-fa10-41b9-89d4-fb41a666537c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MPM |
| Version Model Number | MPM-312-R1 |
| Company DUNS | 948904735 |
| Company Name | CUSTOM ASSEMBLIES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00815849023482 [Primary] |
| LRO | General Surgery Tray |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-21 |
| Device Publish Date | 2023-09-13 |
| 00815849025059 | Procedure Kit |
| 00815849025042 | Procedure Kit |
| 00815849025035 | Procedure Kit |
| 00815849025028 | Procedure Kit |
| 00815849025004 | Procedure Kit |
| 00815849024946 | Procedure Kit |
| 00815849024939 | Procedure Kit |
| 00815849024922 | Procedure Kit |
| 00815849024649 | Procedure Kit |
| 00815849024465 | Procedure Kit |
| 00815849024359 | Procedure Kit |
| 00815849024212 | Procedure Kit |
| 00815849024199 | Procedure Kit |
| 00815849023819 | Procedure Kit |
| 00815849023505 | Procedure Kit |
| 00815849023482 | Procedure Kit |