| 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 |