| Primary Device ID | 30040565117165 |
| NIH Device Record Key | 505b2b19-6bf5-45c8-839e-309f9450cdf6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNI-Solve Adhesive Remover 8oz US |
| Version Model Number | 59402500 |
| Catalog Number | 59402500 |
| Company DUNS | 216344051 |
| Company Name | SMITH & NEPHEW MEDICAL LIMITED |
| 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00040565117164 [Primary] |
| GS1 | 30040565117165 [Package] Contains: 00040565117164 Package: Case [12 Units] In Commercial Distribution |
| KOX | Solvent, Adhesive Tape |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-14 |
| Device Publish Date | 2020-09-04 |
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