| Primary Device ID | 00810180844024 |
| NIH Device Record Key | f298b896-9a9a-4eac-91b2-ae67dfda1804 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Stretch Gauze Bandage Roll, Non-Sterile |
| Version Model Number | 3132 |
| Company DUNS | 008124539 |
| Company Name | Dynarex Corporation |
| Device Count | 500 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| 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 | 00616784313238 [Primary] |
| GS1 | 00810180844024 [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 | 2026-03-09 |
| Device Publish Date | 2021-06-21 |
| 00616784313429 | Stretch Gauze Bandage Roll, Non-Sterile, Individually Wrapped, 4"x4.1yd |
| 00616784313320 | Stretch Gauze Bandage Roll, Non-Sterile, Individually Wrapped, 3"x4.1yd |
| 00616784313221 | Stretch Gauze Bandage Roll, Non-Sterile, Individually Wrapped, 2"x4.1yd |
| 00616784310633 | Stretch Gauze Bandage Roll, Non-Sterile, 6"x4.1yd |
| 00616784310435 | Stretch Gauze Bandage Roll, Non-Sterile, 4"x4.1yd |
| 00616784310336 | Stretch Gauze Bandage Roll, Non-Sterile, 3"x4.1yd |
| 00616784310237 | Stretch Gauze Bandage Roll, Non-Sterile, 2"x4.1yd |
| 00810180844031 | Stretch Gauze Bandage Roll, Non-Sterile, Individually Wrapped, 3"x4.1yd |
| 00810180844024 | Stretch Gauze Bandage Roll, Non-Sterile, Individually Wrapped, 2"x4.1yd |