| Primary Device ID | 10891893002281 |
| NIH Device Record Key | b5bcc264-ddb0-4fe2-beae-dee1cee70ccd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nuprep Skin Prep Gel |
| Version Model Number | 10-91; 10-91K |
| Company DUNS | 039143201 |
| Company Name | D. O. WEAVER AND COMPANY |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00891893002284 [Primary] |
| GS1 | 10891893002281 [Package] Contains: 00891893002284 Package: Secondary Carton [24 Units] In Commercial Distribution |
| GS1 | 20891893002288 [Package] Package: Dealer Case [24 Units] In Commercial Distribution |
| GS1 | 30891893002285 [Package] Contains: 00891893002284 Package: Secondary Carton [3 Units] In Commercial Distribution |
| DRX | Electrode, Electrocardiograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-27 |
| Device Publish Date | 2023-11-17 |
| 30891893002247 | Single 25g tube of Nuprep Skin Prep Gel (unit of use). |
| 10891893002281 | Single-use cup of Nuprep Skin Prep Gel (unit of use) |