| Primary Device ID | EBRE430073149 |
| NIH Device Record Key | f7d94d1e-6f4a-4b1b-9c2d-f91f4dacd1f8 |
| Commercial Distribution Discontinuation | 2019-04-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Vario-Soft 3 mini |
| Version Model Number | 43007314 |
| Catalog Number | 43007314 |
| Company DUNS | 341086190 |
| Company Name | bredent GmbH & Co. KG |
| Device Count | 50 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +4907309872451 |
| info@bredent.com |
| Depth | 2 Millimeter |
| Depth | 2 Millimeter |
| Depth | 2 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EBRE430073140 [Primary] |
| HIBCC | EBRE430073148 [Unit of Use] |
| HIBCC | EBRE430073149 [Package] Contains: EBRE430073140 Package: dummy [1 Units] Discontinued: 2016-09-21 Not in Commercial Distribution |
| EGG | ATTACHMENT, PRECISION, ALL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-04-03 |
| Device Publish Date | 2016-09-21 |
| EBRE430073189 | Vario-Soft 3 mini Matrix, green 50 Pieces |
| EBRE430073169 | Vario-Soft 3 mini Matrix, yellow 50 Pieces |
| EBRE430073149 | Vario-Soft 3 mini Matrix, red 50 Pieces |
| EBRE430073179 | Vario-Soft 3 mini Matrix, green 8 Pieces |
| EBRE430073159 | Vario-Soft 3 mini Matrix, yellow 8 Pieces |
| EBRE430073139 | Vario-Soft 3 mini Matrix, red 8 Pieces |
| EBRE430073129 | Vario-Soft 3 mini 13 Parts 1 Assortment |