| Primary Device ID | 07610221016020 |
| NIH Device Record Key | 9fd4af77-1cb7-494c-acbc-49c687ee1bc2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Geistlich Bio-Oss® Flow |
| Version Model Number | 500950 |
| Company DUNS | 480781728 |
| Company Name | Geistlich Pharma AG |
| 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 |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Total Volume | 0.2 Milliliter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07610221016020 [Primary] |
| NPM | Bone Grafting Material, Animal Source |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-09 |
| Device Publish Date | 2025-07-01 |
| 07610221016037 | 500951 |
| 07610221016020 | 500950 |