| Primary Device ID | 00840117332539 |
| NIH Device Record Key | 8bb7fcbc-229d-41a2-a0b8-10472a4c7f1d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sterile Gauze Pad - All Gauze |
| Version Model Number | 3352-10 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| Device Count | 1 |
| 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 | 00840117332522 [Package] Package: MC Master [48 Units] In Commercial Distribution |
| GS1 | 00840117332539 [Package] Contains: 00840117334182 Package: Box [10 Units] In Commercial Distribution |
| GS1 | 00840117334182 [Primary] |
| NAB | Gauze / Sponge,Nonresorbable For External Use |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-02 |
| Device Publish Date | 2024-03-25 |
| 00840117332652 | 4" x 4", 12-ply |
| 00840117332638 | 4" x 4", 12-ply |
| 00840117332614 | 3" x 3", 12-ply |
| 00840117332591 | 3" x 3", 12-ply |
| 00840117332553 | 2" x 2", 12-ply |
| 00840117332539 | 2" x 2", 12-ply |