| Primary Device ID | 00858961791013 |
| NIH Device Record Key | e486179e-d914-4111-bc97-3924b8a824af |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | up & up rigid gas permeable contact lens cleaner |
| Version Model Number | 630380 |
| Catalog Number | FCP-4143 |
| Company DUNS | 006961700 |
| Company Name | TARGET CORPORATION |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00858961791013 [Primary] |
| MCR | Dilator, Cervical, Hygroscopic, Synthetic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-05-01 |
| Device Publish Date | 2019-04-23 |
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