| Primary Device ID | 00850017274075 |
| NIH Device Record Key | 689d5ac3-1fe6-40b9-a112-b87a2a646bee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CellerateRX Surgical |
| Version Model Number | WCI-05-SACRXP |
| Company DUNS | 807043914 |
| Company Name | Sanara Medtech 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 | 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850017274075 [Primary] |
| KGN | Wound Dressing With Animal-Derived Material(S) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-31 |
| Device Publish Date | 2024-05-23 |
| 00850017274082 | CellerateRX® Surgical Activated Collagen® Powder is Type I bovine hydrolyzed collagen and con |
| 00850017274075 | CellerateRX® Surgical Activated Collagen® Powder is Type I bovine hydrolyzed collagen and con |