| Primary Device ID | EZHIC3020700 |
| NIH Device Record Key | 0733ea6c-74c7-43ac-aa80-950466f1a72c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | hydrogum 5 |
| Version Model Number | C302070 |
| Catalog Number | C302070 |
| Company DUNS | 432971034 |
| Company Name | ZHERMACK SPA |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +390425597611 |
| info@zhermack.com |
| Device Size Text, specify | 0 |
| Storage Environment Temperature | Between 5 Degrees Celsius and 27 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EZHIC3020700 [Primary] |
| ELW | MATERIAL, IMPRESSION |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-09 |
| EZHISP500521 | Alginate impression material |
| EZHISP500511 | Alginate impression material |
| EZHISP500501 | Alginate impression material |
| EZHIC3020750 | Alginate impression material |
| EZHIC3020721 | Alginate impression material |
| EZHIC3020711 | Alginate impression material |
| EZHIC3020700 | Alginate impression material |