| Primary Device ID | 04054596735590 |
| NIH Device Record Key | cf58ae1d-e5d5-4e5c-a746-4a68f9ed35f4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 3M™ ESPE™ Impregum™ Penta™ |
| Version Model Number | 31731 |
| Catalog Number | 31731 |
| Company DUNS | 315731711 |
| Company Name | 3M Deutschland GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| 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 | 04054596735590 [Primary] |
| ELW | MATERIAL, IMPRESSION |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-10 |
| Device Publish Date | 2022-08-02 |
| 04054596735873 | 3M™ ESPE™ Impregum™ Penta™ Soft Quick Step Medium Body Polyether Impression Material Int |
| 04054596735712 | 3M™ ESPE™ Impregum™ Penta™ Soft Medium Body Polyether Impression Material Introkit, P317 |
| 04054596735705 | 3M™ ESPE™ Impregum™ Penta™ Soft Heavy Body Polyether Impression Material Intro Kit, P317 |
| 04054596735590 | 3M™ ESPE™ Impregum™ Penta™ Soft Medium Body Polyether Impression Material Refill, 31731 |
| 04054596735569 | 3M™ ESPE™ Impregum™ Penta™ Soft Heavy Body Polyether Impression Material Refill, 31741 |
| 04054596735538 | 3M™ ESPE™ Impregum™ Penta™ H Soft Quick Step Polyether Impression Material Refill, 31769 |
| 04054596735521 | 3M™ ESPE™ Impregum™ Penta™ Soft Light Body Polyether Impression Material Refill, 31746 |