| Primary Device ID | EBGOFLPCA301 |
| NIH Device Record Key | 04b464a1-6e39-4577-a2f6-98b09d944f38 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Permanent Crown A3 |
| Version Model Number | FLPCA301US |
| Company DUNS | 316483072 |
| Company Name | BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com | |
| Phone | +4942120280 |
| info@bego.com |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EBGOFLPCA301 [Primary] |
| EBF | Material, Tooth Shade, Resin |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-27 |
| Device Publish Date | 2020-10-19 |
| EBGOFLPCA301 | FLPCA301US |
| EBGOFLPCA301US1 | FLPCA301US |