| Primary Device ID | 00848956003191 |
| NIH Device Record Key | 00179d90-9e4e-4f35-adbf-9dc9cca9ebeb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Face shield |
| Version Model Number | SHL-003 |
| Catalog Number | SHL-003 |
| Company DUNS | 057680480 |
| Company Name | HEALTHMARK INDUSTRIES CO., INC. |
| Device Count | 20 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00848956003191 [Unit of Use] |
| GS1 | 10848956003198 [Primary] |
| LYU | Accessory, Surgical Apparel |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-15 |
| Device Publish Date | 2022-12-07 |
| 00848956003016 | SHL-002 |
| 00848956003191 | SHL-003 |
| 00848956002774 | SHL-001 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FACE SHIELD 87103115 5279347 Live/Registered |
TDS Management, Inc. 2016-07-13 |
![]() FACE SHIELD 78634151 not registered Dead/Abandoned |
Sally Hershberger Face Place Laboratories, Inc. 2005-05-20 |
![]() FACE SHIELD 73498401 1341991 Dead/Cancelled |
MENTHOLATUM COMPANY, THE 1984-09-10 |
![]() FACE SHIELD 73220472 1157112 Dead/Cancelled |
Hudson Oxygen Therapy Sales Company 1979-06-21 |