| Primary Device ID | 00197644272952 |
| NIH Device Record Key | fd3e4782-8211-4e1e-8965-ac0b23421e36 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Scarguard® Labs Vitamin E Sheets |
| Version Model Number | None |
| Company DUNS | 009778989 |
| Company Name | Blh Pharmaceuticals Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00197644272952 [Primary] |
| MDA | Elastomer, Silicone, For Scar Management |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-11 |
| Device Publish Date | 2024-12-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SCARGUARD 90527290 not registered Live/Pending |
Velius, LLC 2021-02-12 |