| Primary Device ID | 00810120952208 |
| NIH Device Record Key | 5b39ffba-60d9-4a38-b108-7cd9dd571ee4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ADVANCE IF 41 |
| Version Model Number | BPF-41XXL |
| Company DUNS | 052262122 |
| Company Name | Diamond Gloves |
| Device Count | 100 |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810120952185 [Unit of Use] |
| GS1 | 00810120952192 [Primary] |
| GS1 | 00810120952208 [Package] Contains: 00810120952192 Package: [10 Units] In Commercial Distribution |
| 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 | 2024-01-25 |
| Device Publish Date | 2024-01-17 |
| 00810120952208 | IF 41 Powder Free Nitrile Examination Gloves, (Black) XX-LARGE |
| 00810120952178 | IF 41 Powder Free Nitrile Examination Gloves, (Black) X-LARGE |
| 00810120952147 | IF 41 Powder Free Nitrile Examination Gloves, (Black) LARGE |
| 00810120952116 | IF 41 Powder Free Nitrile Examination Gloves(Black) MEDIUM |
| 00810120952086 | IF 41 Powder Free Nitrile Examination Gloves (Black) , SMALL |
| 00810120952055 | IF 41 Powder Free Nitrile Examination Gloves (Black) X-SMALL |