| Primary Device ID | 00810180840699 |
| NIH Device Record Key | 91fcfe34-4c36-45b2-a61a-c48027357202 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DynaSafety Compress Bandages,3", Offset, Sterile |
| Version Model Number | 3193 |
| Company DUNS | 008124539 |
| Company Name | Dynarex Corporation |
| Device Count | 800 |
| 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 | true |
| 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 | 00616784319339 [Primary] |
| GS1 | 00810180840699 [Unit of Use] |
| FQM | Bandage, Elastic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-10-30 |
| Device Publish Date | 2021-06-21 |
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