| Primary Device ID | 00850049592437 |
| NIH Device Record Key | fc8a2157-c776-408e-8378-e7f323d92ae4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | sup medic |
| Version Model Number | SKF01304 |
| Company DUNS | 107150886 |
| Company Name | Supmedics 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850049592437 [Primary] |
| LZA | Polymer Patient Examination Glove |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-23 |
| Device Publish Date | 2025-05-15 |
| 00810160181637 - supmedic | 2025-05-23 |
| 00810160181644 - supmedic | 2025-05-23 |
| 00810160181651 - supmedic | 2025-05-23 |
| 00810160181668 - supmedic | 2025-05-23 |
| 00850049592413 - supmedic | 2025-05-23 |
| 00850049592420 - supmedic | 2025-05-23 |
| 00850049592437 - sup medic | 2025-05-23 |
| 00850049592437 - sup medic | 2025-05-23 |
| 00850049592444 - supmedic | 2025-05-23 |