| Primary Device ID | 06973133310152 |
| NIH Device Record Key | daddf0d4-0b97-4188-98f1-b2cbee8dcc33 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ZCG ZR Procelain |
| Version Model Number | Dentine B1M1 |
| Company DUNS | 560453518 |
| Company Name | BAOT Biological Technology Co., Ltd. |
| 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 | 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 | 06973133310152 [Primary] |
| EIH | Powder, Porcelain |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-22 |
| Device Publish Date | 2020-05-14 |
| 06973133310176 | It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full |
| 06973133310169 | It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full |
| 06973133310152 | It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full |
| 06973133310145 | It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full |
| 06973133310138 | It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full |
| 06973133310121 | It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full |