| Primary Device ID | EKUR1060010KA0 |
| NIH Device Record Key | 69ca5952-18ec-4deb-a95f-2f82899bec49 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCREENING PORCELAIN |
| Version Model Number | 106-0010KA |
| Company DUNS | 697119498 |
| Company Name | KURARAY NORITAKE DENTAL INC. |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EKUR1060010KA0 [Primary] |
| EIH | Powder, Porcelain |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-24 |
| Device Publish Date | 2017-02-17 |
| EKUR1060201KA0 | SR GRAY 10g |
| EKUR1060191KA0 | S BROWN 10g |
| EKUR1060181KA0 | MR GLAY 10g |
| EKUR1060171KA0 | M BROWN 10g |
| EKUR1060161KA0 | GIL 10g |
| EKUR1060151KA0 | GM WHITE 10g |
| EKUR1060141KA0 | GM ORANGE 10g |
| EKUR1060131KA0 | NW0.5G 10g |
| EKUR1060121KA0 | NW0G 10g |
| EKUR1060111KA0 | D3G 10g |
| EKUR1060101KA0 | D2G 10g |
| EKUR1060091KA0 | C2G 10g |
| EKUR1060081KA0 | C1G 10g |
| EKUR1060071KA0 | B3G 10g |
| EKUR1060061KA0 | B2G 10g |
| EKUR1060051KA0 | B1G 10g |
| EKUR1060041KA0 | A3G 10g |
| EKUR1060031KA0 | A2G 10g |
| EKUR1060021KA0 | A1G 10g |
| EKUR1060010KA0 | SCREENING PORCELAIN KIT 170g |